An emergency recall of children’s cough suppressants has been issued by Novis PR, LLC after it was found that some packages contain a lethal combination of ethyl alcohol and benzocaine. Consumption of the drug by children can result in near immediate coma and death. As of the writing of this notice, no adverse effects have yet been reported, but it is imperative that all consumers who utilize the drops check their packages immediately.

SUMMARY

Date of Recall:

Announced: May 18, 2023

Public Notification: May 19, 2023

Name(s) of Drug:

G-SUPRESS DX

Company Name:

Novis PR, LLC

Drug Indication:

Pediatric Cough Suppressant

Pediatric Expectorant

Pediatric Nasal Decongestant

Common Cold

Product Description

The drops are packaged in 0.5oz and 1 oz bottles that are sold in carton boxes. Packages also include the phrase, “Sugar & Alcohol FREE.” Product was distributed throughout Puerto Rico. The Spanish version of the FDA notice can be found here.

Reason for Recall

During manufacturing a product other than the intended drops was placed into the bottles. Ethyl Alcohol and Benzocaine, which can cause deadly side effects were packaged into the bottles without appropriate labeling. The cause of the mix-up has not yet been released.

Impacts

Infants and children who consume ethyl alcohol can develop hypoglycemic coma or hypothermia which may result in death if not treated immediately and aggressively in a medical setting. All consumers who utilize the product are at risk for developing methemoglobinemia, a rare blood disorder leading to:

• Cyanosis (blue skin)
• Pallor (pale skin)
• Fatigue (tiredness)
• Weakness
• Headache
• Lack of Coordination
• Poor Judgment
• Slow Breathing
• Confusion
• Slurred Speech
• Seizures
• Irregular Heart Rhythm
• Coma
• Death

Lot information

Consumers who have purchased G-SUPRESS DX should locate the box and bottle and find the lot number. If the lot number matches the number listed below, the medication is part of the recall. See below for further instructions.

FDA.gov

Have you found that your medication is part of the recall? Here’s what you should do:

Consumers

If you find that your lot of medication is part of this recall, do the following:

1. DISCONTINUE USE OF THIS PRODUCT IMMEDIATELY.
2. Notify your physician or pediatrician immediately if any of the recalled product has been consumed.
3. Continue to monitor your health for any adverse symptoms over the next week and notify your physician if any concerns are noted.
4. Consumers may contact Novis PR LLC at 787-767-2072. They are available Mon-Fri from 8:00am to 4:00pm (EST). No email address has been provided.
5. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
6. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Novis PR LLC at 787-767-2072. They are available Mon-Fri from 8:00am to 4:00pm (EST). Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Novis PR LLC at 787-767-2072. They are available Mon-Fri from 8:00am to 4:00pm (EST). Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

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Nature’s Energy has issued a voluntary and immediate recall of their Children’s Chewable Colostrum supplements due to the presence of milk proteins in its packaging. While no adverse reactions have been reported as of the writing of this notice, the presence of milk can present a danger to those with milk allergies. It is imperative that anyone with an allergy to milk stop using this recalled product immediately.

SUMMARY

Date of Recall:

Announced: May 18, 2023

Public Notification: May 18, 2023

Name(s) of Drug:

Nature’s Energy Children’s Chewable Colostrum

Company Name:

Nature’s Energy

Drug Indication:

Children’s nutritional supplement

Product Description

The supplements were packaged in white, plastic bottles with a blue label featuring a cartoon cow. Various flavors all depict symbolism related to the flavor such as berries, candies or creamsicle pops. Each bottle contains 180 chewable tablets.

Products were sold to consumers via Amazon and the Nature’s Energy website.

Reason for Recall

The supplement’s package did not indicate that it could contain the presence of milk proteins and therefore present a danger to those with a milk allergy.

Impacts

Those with milk allergies who consume milk proteins can experience dangerous symptoms including:

• Stomach Pain
• Vomiting
• Diarrhea
• Constipation
• Rash
• Swelling of Face and Lips
• Runny Nose
• Wheezing
• Shortness of Breath
• Anaphylaxis and Death

IF SOMEONE EXPERIENCES SYMPTOMS SUCH AS SHORTNESS OF BREATH, NOISY BREATHING, LOSS OF CONSCIOUSNESS, SEIZURES OR ANY OTHER LIFE-THREATENING SYMPTOMS, CALL 911 IMMEDIATELY.

Lot information

Consumers should locate the lot number and expiration date printed on the bottom of the supplement bottle. Then, utilize the chart below to determine if each bottle is included in the recall.

FDA.gov

Have you found that your supplement is part of the recall? Here’s what you should do:

Consumers

If you find that your supplement is part of this recall, do the following:

1. Discontinue use of the supplement immediately.
2. Continue to monitor your child’s health for any adverse symptoms over the next week and notify your physician if any concerns are noted.
3. Return the product to the place of purchase for a refund.
4. Consumers may contact Nature’s Energy at 801-785-2304. They are available Mon-Fri from 8:00am to 4:00pm (MT). You can also contact them via email at admin@naturesenergy.us.
5. If your child is currently experiencing or has experienced an adverse reaction to this medication (listed above), notify your pediatrician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
6. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Nature’s Energy at 801-785-2304 or you can utilize admin@naturesenergy.us to contact them via email. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Nature’s Energy at 801-785-2304 or use admin@naturesenergy.us to contact them via email. Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

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An additional voluntary recall has been issued by Perrigo for limited quantities of their Gerber Good Start SoothePro TM Powdered Infant Formula after previously recalled formula continued to be distributed to and sold at retailers throughout multiple states. Initially, the recall was posted due to possible presence of Cronobacter Sakazakii bacteria which can lead to fever, poor feeding, excessive crying or low energy in infants who are exposed. At this time of this notice, no adverse events have been reported and no formula has tested positive for the bacteria, but out of an abundance of caution, the company has chosen to move forward with the recall.

SUMMARY

Date of Recall:

Announced: March 17, 2023 Repeated: May 13, 2023

Public Notification: March 17, 2023 Repeated: May 14, 2023

Name(s) of Product:

Gerber Good Start SoothePro TM Powdered Infant Formula

Company Name:

Perrigo

Indication:

Infant feeding

Product Description

Product is distributed in 12.4oz cans with a blue lid and Gerber logo on the front.

Reason for Recall

Initial Recall: There is reason to suspect that the formula processed in a Wisconsin manufacturing plant may have been exposed to the Cronobacter Sakazakii bacteria. While the bacteria does not cause any symptoms in healthy adults, it can be problematic for infants, especially those who are premature or immunocompromised. View initial recall here.

Current Recall: After the initial recall was announced, it was noted that the recalled formula continued to be distributed by the Nashville Division to multiple retailers throughout Alabama, Georgia, Indiana, Kentucky, Ohio, Tennessee, Virginia and West Virginia. The recalled formula was then sold at the following independent retailers:

• • • Belle Foods
    • Bellview Price Cutter
    • Booneville Shopwise
    • Brown County IGA
    • Buehler’s
    • Buehler’s Cash Saver
    • Buehler’s IGA
    • Camridge City Market
    • Campbell’s Market
    • Crossroads IGA
    • Food City
    • Food Giant
    • Food World
    • Foodland
    • Frabergs Foods
    • Fresh N Low
    • Gallion’s Market
    • Gregerson’s Cash Saver
    • Hilltop Cee Bee
    • Hometown IGA
    • Houchen’s
    • Howards’s IGA
    • Laurel Grocery Company
    • Liberty IGA
    • Market Place
    • Noble’s Price Cutter
    • Price Less Foods
    • Price Less IGA
    • Quality Foods
    • Riesbeck’s
    • Rivertown IGA
    • Simpson’s Supermarket
    • Spencer Cash Saver
    • Stop to Save
    • Sureway
    • Sureway Henderson
    • Swafford and Sons IGA
    • Tietgens Mt. Pleasant IGA
    • Valu Market
    • Versailles IGA
    • Vevay IGA
    • Village Market & Café
    • Walnut Creek Country Market
    • Winburn Fruit Market
    • Woodruff’s Supermarket

Impacts

Infants fed the formula may experience fever, poor feeding, excessive crying or low energy as a result of exposure to the bacteria.

Lot information

Consumers should locate their can of formula and check for “use by” dates as well as lot codes located on the bottom of the package. Only the following listed lots and use by dates are affected.

Gerber® Good Start® SootheProTM 12.4 oz:
300357651Z – USE BY 04JUL2024
300457651Z – USE BY 05JUL2024
300557651Z – USE BY 06JUL2024
300557652Z – USE BY 06JUL2024
300757651Z – USE BY 08JUL2024
300857651Z – USE BY 09JUL2024
301057651Z – USE BY 11JUL2024
301057652Z – USE BY 11JUL2024
301157651Z – USE BY 12JUL2024

Fda.gov

Have you found that your formula is part of the recall? Here’s what you should do:

Consumers

If you find that your lot of formula is part of this recall, do the following:

1. Stop feeding your child this formula immediately and replace with a formula that is not part of the recall (note that this recall applies to only a small number of lots and expiration dates)
2. Continue to monitor your baby’s health for any adverse symptoms over the next week and notify their physician if any concerns are noted.
3. Consumers should contact the Gerber Parent Resource Center at 1-800-777-7690 for a refund. They are available 24/7.
4. If your child is currently experiencing or has experienced an adverse reaction to this formula (listed above), notify your child’s physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
5. Contact MedWaste Management for information and/or assistance with disposing of the recalled formula.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Gerber Parent Resource Center at 1-800-777-7690. They are available 24/7. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled formula.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Gerber Parent Resource Center at 1-800-777-7690. They are available 24/7.
3. Notify them of any recalled batches that have already been shipped to retailers.
4. Notify affected retailers of recalled batches that they have already or will receive.
5. Contact MedWaste Management for information and/or assistance with disposing of the recalled formula.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

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Advil, a popular over-the-counter medication used for pain relief is being recalled nationwide due to concerns that the medication was stored at temperatures outside of required guidelines. This recall applies only to Advil sold at Family Dollar stores in the United States. Advil distributed by any other organization is not affected by the recall at this time. As of the writing of this notice, no adverse events related to the issue have yet been reported.

SUMMARY

Date of Recall:

Announced: May 4, 2023

Public Notification: May 4, 2023

Name(s) of Drug:

Advil (multiple formulations affected, see chart below)

Company Name:

Family Dollar Stores

Drug Indication:

Pain

Product Description

The medication was sold in boxes or bottles clearly labeled with the name of the medication.

Reason for Recall

Improperly storing medications and exposing them to temperatures higher or lower than recommended can cause the medication to break down and become less effective. In some cases, medications can become toxic.

Impacts

Consumers who have purchased an effected batch of the medication and who continue to utilize it may experience lack of symptom relief.  Additionally, some side effects could be extreme due to toxicity associated with the breakdown of the medication.

Lot information

Medications associated with this recall were sold between (or around) June 1, 2022 to March 31, 2023.

Consumers should locate the box or bottle in which the medication comes to compare SKU and batch numbers with the chart below. If you find your SKU and batch number on the chart below, your medication is affected by the recall and you will need to take additional steps in order to ensure that your health is not affected and to take part in recall procedures.

FDA.gov

Have you found that your medication is part of the recall? Here’s what you should do:

Consumers

If you find that your lot of medication is part of this recall, do the following:

1. Discontinue use of the medication immediately.
2. Monitor your health for any adverse symptoms and notify your physician if any concerns are noted.
3. Consumers may return the unused portion of the medication to the Family Dollar store where they purchased it for a full refund. Receipts are not necessary for refunds in this case. Consumers may also contact Family Dollar customer service at 1-844-636-7687. They are available from 9am to 5pm EST.
4. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
5. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

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Teva Pharmaceuticals USA has issued an immediate recall of certain lots of Fentanyl Buccal (placed in cheek) Tablets CII due to missing information in the product insert. Lack of proper safety information within the insert can lead to serious health ramifications due to mis-use by consumers. As of the writing of this notice, no adverse events have yet been reported.

SUMMARY

Date of Recall:

Announced: April 27, 2023

Public Notification: April 28, 2023

Name(s) of Drug:

Fentanyl Buccal Tablets CII

Company Name:

Mayne Pharma, Inc. (brand)

Teva Pharmaceuticals USA (manufacturer)

Drug Indication:

Pain

Product Description

Product is packaged in white boxes with a single orange, green, blue, pink or yellow stripe. The box contains 7 cards, each containing 4 tablets. Each tablet within the card is encased in a foil lined, childproof blister. Each tablet is a flat, white, round tablet debossed with a “C” on one side and a 1, 2, 4, 6 or 8 on the other.

Reason for Recall

Updates made to the products insert and medication guide were omitted and potentially leave room for the consumer to receive mis-information that can lead to improper use of this potentially dangerous medication.

Impacts

Consumers who receive mis-information could potentially receive an incorrect dose of the medication. Receiving less than prescribed doses of the medication could lead to continued symptoms or symptoms of withdrawal (see below). For consumers receiving more than the prescribed dose, symptoms could include:

• Pinpoint Pupils
• Slurred Speech
• Inability to Walk Properly
• Falling Asleep
• Loss of Consciousness
• Cold, Clammy Skin
• Slowed Breathing
• Complete Lack of Breathing
• Death

Lot information

Consumers should locate the box in which the medication comes to compare NDC and lot numbers as well as expiration dates, strength, and size with the chart below. If you find your NDC number, lot number, strength, size and expiration date on the chart below, your medication is affected by the recall and you will need to take additional steps in order to ensure that your health is not affected and to take part in recall procedures.

FDA.gov

Have you found that your medication is part of the recall? Here’s what you should do:

Consumers

NOTE: CONSUMERS SHOULD NOT DISCONTINUE THIS MEDICATION ABRUPTLY. SPEAK TO YOUR DOCTOR BEFORE MAKING ANY CHANGES.

Discontinuation of this medication may cause return of pain symptoms or symptoms of Fentanyl withdrawal. These may include:

• Diarrhea
• Sweating
• Insomnia
• Dilated Pupils
• Nausea
• Sweating
• Fever
• Intense Cravings for Fentanyl

If you find that your lot of medication is part of this recall, do the following:

1. Call your doctor right away. Ask for a new prescription to replace your recalled medication and report any changes in your symptoms.
2. Notify your physician of any change in your health.
3. Once you have obtained a replacement for your medication, Teva is asking that you return any unused portion of the medication. Consumers should contact Teva at 1-855-246-5024 or via email at rxrecalls@inmar.com for assistance with returns.
4. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately. Once you have sought medical assistance, please notify the pharmaceutical company at 1-888-483-8279 or contact them via email at USMedInfo@tevapharm.com. You may also notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
5. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact IBSA Pharma Inc at 1-855-246-5024 or via email at rxrecalls@inmar.com. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact IBSA Pharma Inc at 1-855-246-5024 or via email at rxrecalls@inmar.com. Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

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A nationwide recall of various popular weight loss supplements has been issued. TruVision Health has voluntarily issued the recall after it was found that their supplements contain unapproved dietary ingredients (Hordenine and Octodrine/DMHA) that can cause serious side effects for those who consume them. At highest risk are pregnant women and those who heart conditions.

As of the writing of this notice, no deaths have been reported, but consumers have experienced chest pain, chills, diarrhea, lightheadedness, fatigue, cephalalgia (headache), hypertension (high blood pressure), tachycardia (high heart rate), jitters, nausea, anxiety (nervousness), dermatitis (rash), stomach pain, upset stomach, diaphoresis (sweating) and emesis (vomiting).

SUMMARY

Date of Recall:

Announced: April 27, 2023

Public Notification: April 27, 2023

Name(s) of Drug:

Various drugs sold under the following brand names:

Truvy

TruVision

reFORM

Company Name:

TruVision Health

Drug Indication:

Dietary Supplements

Weight Loss Supplements

Product Description

Each supplement was sold in capsule form and packaged in blister packs attached to cardboard cartons or as stick packs that were sold in counts of 30. Products were sold online by Truvy.com.

Reason for Recall

Consumers are experiencing serious side effects such as tachycardia (high heart rate) and hypertension (high blood pressure) that have major health consequences for those with heart conditions and pregnant women. Even healthy consumers without any underlying conditions could be seriously affected by the ingestion of these supplements.

Impacts

As stated above, consumers have experienced chest pain, chills, diarrhea, lightheadedness, fatigue, cephalalgia (headache), hypertension (high blood pressure), tachycardia (high heart rate), jitters, nausea, anxiety (nervousness), dermatitis (rash), stomach pain, upset stomach, diaphoresis (sweating) and emesis (vomiting) after ingestion of the supplements.

Lot information

Consumers should locate the package in which their supplement in housed and compare the product description as well as the SKU and lot numbers below to confirm if their supplement is included in the recall.

FDA.gov

Have you found that your medication is part of the recall? Here’s what you should do:

Consumers

If you find that your lot of medication is part of this recall, do the following:

1. Discontinue use of the supplement immediately.
2. Call your doctor right away. Report any changes in your health that you have experienced while taking the supplements. Notify your doctor that your supplement is part of the recall.
3. Continue to monitor your health for any adverse symptoms over the next week and notify your physician if any concerns are noted.
4. Consumers should contact TruVision Health, LLC for a full refund. They can be contacted via telephone at 1-855-213-8788 and are available Mon-Fri from 7:00am-6:00pm (MDT).
5. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
6. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

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Akorn Operating Company, LLC has declared bankruptcy and discontinued all operations including their quality program. This has resulted in an inability to identify if products being distributed to the public are safe for consumption and use. Products could be contaminated with unintended substances, could vary in strength, or could contain other quality discrepancies that may affect the health of those who receive them. Therefore, all of their products are being recalled immediately. As of the writing of this notice, no adverse effects have yet been reported.

SUMMARY

Date of Recall:

Announced: April 26, 2023

Public Notification: April 26, 2023

Name(s) of Drug:

See Chart Below

Company Name:

Akorn Operating Company, LLC

Drug Indication:

See Chart Below

Product Description

See Chart Below

Reason for Recall

Quality control measures are imperative in maintaining the appropriate strength and specifications of each medication. Without it, medications may contain harmful substances or discrepancies in quality control that can affect the way the medications react within the human or animal body. No adverse effects have yet been reported and at this time this recall is being issued out of caution only.

Impacts

Consumers who utilize the medications listed may be receiving a higher or lower dose than indicated, or could be ingesting substances that have contaminated the medications during the manufacturing process. This could lead to serious health outcomes including (but not limited to) allergic reactions, increase or decrease in underlying symptoms, organ damage, or even death.

Lot information

For each medication listed, all NDCs and all lots are being recalled. Each medication was packaged by Akorn. If your medication was produced or packaged elsewhere, it is not currently part of this particular recall. All listed medications, even if they are not currently expired, are included in the recall.

Medications were distributed nationwide through wholesalers, retailers, medical facilities and online sellers. Please check all of your medications.

HUMAN PRODUCTS

ANIMAL PRODUCTS

Have you found that your medication is part of the recall?

Here’s what you should do:

Consumers

If you find that your lot of supplements is part of this recall, do the following:

1. DO NOT DISCONTINUE USE OF THE MEDICATION UNTIL YOU HAVE SPOKEN TO YOUR PHYSICIAN OR VETERINARIAN. SOME MEDICATIONS HAVE SERIOUS SIDE EFFECTS WHEN STOPPED SUDDENLY. NOTIFY YOUR PHYSICIAN/VETERINARIAN IMMEDIATELY IF YOUR MEDICATION IS INCLUDED IN THE RECALL.
2. Request a replacement prescription from your physician.
3. Notify your physician/veterinarian if you or your pet has utilized the medication and have experienced any of the symptoms listed above.
4. Continue to monitor your health and the health of any pets who have received listed medications for any adverse symptoms over the next week and notify your physician/veterinarian if any concerns are noted.
5. Consumers may request a refund from the location at which they purchased their product. They may also contact the manufacturer by telephone at 1-800-932-5676. They are available Monday-Friday from 8am-5pm (CDT).
6. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form. For pets who experience an adverse reaction, the FDA reporting form can be found here.
7. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact the manufacturer by telephone at 1-800-932-5676. They are available Monday-Friday from 8am-5pm (CDT). Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact the manufacturer by telephone at 1-800-932-5676. They are available Monday-Friday from 8am-5pm (CDT). Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

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A voluntary nationwide recall has been issued for Pro Power Knight Plus, NUX Male Enhancement and DYNAMITE SUPER capsules. Contaminants Sildenafil and Tadalafil have been found in the supplements and could lead to serious consequences such as dangerous interactions with prescriptions drugs and life-threatening hypotension (low blood pressure). As of the writing of this notice, no adverse effects have yet been reported.

SUMMARY

Date of Recall:

Announced: April 26, 2023

Public Notification: April 26, 2023

Name(s) of Drug:

Pro Power Knight Plus

NUX

Dynamite Super

Company Name:

Gadget Island, Inc.

Drug Indication:

Erectile Dysfunction

Product Description

Each capsule is packaged individually in a clear clamshell that is attached to a black, cardboard card. Capsules are blue or red in color. Packages were sold nationwide in retail locations and sold at www.gearisle.com.

Reason for Recall

The pills are contaminated with unapproved substances (Sildenafil and Tadalafil) which react with common medications used for heart conditions, diabetes and high cholesterol.

Impacts

Consumers experiencing an interaction between the pills and their medication may experience symptoms of hypotension (low blood pressure) including weakness, lightheadedness, fainting, confusion, blurred vision, nausea, vomiting and even DEATH. In particular, those who take the following medications are at high risk of interaction.

• Nitroglycerin
• Nitrostat
• Nitromist
• Nitrolingual Pumpspray
• Nitro-Bid
• Nitropress
• Nitroprusside
• Nitro-Dur
• Transderm-Nitro
• Nitro-Time
• Isosorbide Mononitrate
• Dinitrate
• Isordil
• Isordil Titradose
• Dilatrate-SR
• Amyl Nitrite
• Amyl Nitrate

Lot information

To identify whether or not your capsules are part of the recall, locate the package in which it is sold and locate the product name, UPC, Lot # and Expiration Date, then compare to the chart below.

Fda.gov

Have you found that your supplement is part of the recall?

Here’s what you should do:

Consumers

If you find that your lot of supplements is part of this recall, do the following:

1. STOP USING THE SUPPLEMENT IMMEDIATELY!
2. Notify your physician if you have utilized the medication and have experienced any of the symptoms listed above.
3. Continue to monitor your health for any adverse symptoms over the next week and notify your physician if any concerns are noted.
4. Consumers may request a full refund from the location at which they purchased their product. They may also contact the manufacturer by telephone at 1-888-387-4753 or via email at info@gearisle.com.
5. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
6. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact the manufacturer by telephone at 1-888-387-4753 or info@gearisle.com via email. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact the manufacturer by telephone at 1-888-387-4753 or via email at info@gearisle.com. Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

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An immediate recall of Terry Naturally BioActive Vitamin B and EuroMedica Active B Complex supplements has been issued due to the presence of undeclared milk. EuroPharma, Inc. has issued this recall out of an abundance of caution, though no adverse events have yet been reported.

SUMMARY

Date of Recall:

Announced: April 21, 2023

Public Notification: April 22, 2023

Name(s) of Drug:

Terry Naturally BioActive Vitamin B

EuroMedica Active B Complex.

Company Name:

EuroPharma, Inc.

Drug Indication:

Supplement marketed to the general public for improvement of brain and cognitive function, heart health and nervous system function.

Product Description

Supplements are packaged in white, plastic bottles. Labels are white and orange or white and blue. Each bottle contains 60 capsules.

Reason for Recall

The supplements have been found to contain milk. However, they are labeled as vegan in some cases and in others, milk is not declared. For those with milk sensitivity or allergies, this can lead to serious health impacts.

Impacts

Consumers with an allergy to milk who continue to ingest the supplements could experience an allergic reaction. Symptoms are not limited to but can include:

• Rash
• Swelling of Face and Lips
• Stomach Pain
• Vomiting
• Diarrhea
• Constipation
• Runny Nose
• Wheezing
• Shortness of Breath
• Anaphylaxis and Death

IF YOU OR A LOVED ONE EXPERIENCES A REACTION THAT CAUSES SHORTNESS OF BREATH, NOISY BREATHING, LOSS OF CONSCIOUSNESS, SEIZURES OR ANY OTHER LIFE-THREATENING SYMPTOMS, CALL 911 IMMEDIATELY.

Lot information

Consumers should locate the box in which the medication comes to compare NDC and lot numbers as well as expiration dates with the chart below. If you find your NDC number, lot number and expiration date on the chart below, your medication is affected by the recall and you will need to take additional steps in order to ensure that your health is not affected and to take part in recall procedures.

FDA.gov

Have you found that your supplement is part of the recall? Here’s what you should do:

Consumers

If you find that your supplement is part of this recall, do the following:

1. Discontinue use of the supplement immediately.
2. Call your doctor right away if any symptoms of an adverse reaction are noted.
3. Continue to monitor your health for any adverse symptoms over the next week and notify your physician if any concerns are noted.
4. Consumers may return the product to place of purchase for a full refund.
5. Consumers may also contact EuroPharma, Inc. at 1-920-593-3729. They are available Mon-Fri from 8:00am to 4:00pm (CST). You can also contact them via email at qualitydept@europharmausa.com.
6. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
7. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact EuroPharma, Inc. at 1-920-593-3729 or you can utilize qualitydept@europharmausa.com to contact them via email. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact EuroPharma, Inc. at 1-920-593-3729 or you can utilize qualitydept@europharmausa.com to contact them via email. Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

Medical Waste Disposal Services

MedWaste’s Blog Index

Medical Waste Regulations

MedWaste’s Product Store

Learn How To Properly Manage & Dispose of Household Medical Waste

Rico Perez Products, Inc. has issued an immediate recall of their Super Kids Colostrum supplements due to the undeclared presence of milk, a common allergen. Children who are receiving the supplement, but have an allergy to milk are at danger of experiencing a serious or even life-threatening reaction. At the time of the writing of this notice, no reactions or deaths have been reported.

SUMMARY

Date of Recall:

Announced: April 13, 2023

Public Notification: April 13, 2023

Name(s) of Drug:

Super Kids Colostrum, Dietary Supplement

Company Name:

Rico Perez Products, Inc.

Drug Indication:

Children’s nutritional supplement

Product Description

The supplements were packaged in white, plastic bottles with a cow-patterned label affixed. Each label indicates, “Dr. Rico Perez Super Kids Colostrum” and contains 60 chewable tablets.

Reason for Recall

The supplements were labeled without indication that they contain the allergen, milk.

Impacts

Children with a milk allergy who continue to receive the supplements could experience an allergic reaction. Symptoms are not limited to but can include:

• Rash
• Swelling of Face and Lips
• Stomach Pain
• Vomiting
• Diarrhea
• Constipation
• Runny Nose
• Wheezing
• Shortness of Breath
• Anaphylaxis and Death

IF YOUR CHILD EXPERIENCES A REACTION THAT CAUSES THEM TO HAVE SHORTNESS OF BREATH, NOISY BREATHING, LOSS OF CONSCIOUSNESS, SEIZURES OR ANY OTHER LIFE-THREATENING SYMPTOMS, CALL 911 IMMEDIATELY.

Lot information

Consumers should locate their bottle of Super Kids Colostrum supplements and locate the UPC code, lot number and expiration date, which are likely located on the bottom of the bottle. Compare with the chart below to identify if your supplements is part of the recall.

FDA.gov

Have you found that your supplement is part of the recall? Here’s what you should do:

Consumers

If you find that your supplement is part of this recall, do the following:

1. Discontinue use of the supplement immediately.
2. Continue to monitor your child’s health for any adverse symptoms over the next week and notify your physician if any concerns are noted.
3. Return the product to the place of purchase for a refund.
4. Consumers may contact Rico Perez Products at 305-856-5304. They are available Mon-Fri from 10:00am to 6:00pm (EST). You can also contact them via email at info@ricoperez.com.
5. If your child is currently experiencing or has experienced an adverse reaction to this medication (listed above), notify your pediatrician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
6. Contact MedWaste Management for information and/or assistance with disposing of the recalled supplement.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Rico Perez Products, Inc. at 305-856-5304 or you can utilize info@ricoperez.com to contact them via email. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Rico Perez Products, Inc. at 305-856-5304 or use info@ricoperez.com to contact them via email. Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

Medical Waste Disposal Services

MedWaste’s Blog Index

Medical Waste Regulations

MedWaste’s Product Store

Learn How To Properly Manage & Dispose of Household Medical Waste

Camber Pharmaceuticals, Inc has issued a nationwide recall of their oral suspension of Atovaquone (a generic drug commonly substituted for Mepron) due to possible contamination with Bacillus Cereus, a dangerous bacteria. Atovaquone is commonly subscribed to treat PCP (Pneumocystis Pneumonia), a fungal infection of lungs caused by Pneumocystis Jirovecii, in patients who are unable to be treated with first line therapies such as Trimethoprim-Sulfamethoxazole (a generic medication commonly substituted for Bactrim or Septra). As of the writing of this notice, no adverse events have been reported.

SUMMARY

Date of Recall:

Announced: March 13, 2023

Public Notification: March 31, 2023

Name(s) of Drug:

Atovaquone

Company Name:

Chamber Pharmaceuticals, Inc.

Drug Indication:

PCP (Pneumocystis Pneumonia)

Fungal Infections

Product Description

The oral solution is by prescription only and is packaged in standard white bottles that hold 210 mL of liquid.

Reason for Recall

The drug could possibly be contaminated with Bacillus Cereus, a bacteria that can cause deadly infections including endocarditis (inflammation of the lining of the heart) and necrotizing soft tissue infections.

Impacts

Consumers who have received an effected batch of the medication and who continue to utilize it may experience symptoms such as:

• Vomiting
• Diarrhea
• Fever
• Chills
• Sweats
• Weakness
• Fatigue
• Aches & Pains in Muscles/Joints
• Shortness of Breath with Activity
• Swelling of Feet, Legs or Abdomen
• Skin Infections that become increasingly painful or hot or begin to drain a grey liquid.

Lot information

Consumers should locate the bottle in which the medication comes to compare NDC and lot numbers as well as expiration dates with the chart below. If you find your NDC number, lot number and expiration date on the chart below, your medication is affected by the recall and you will need to take additional steps in order to ensure that your health is not affected and to take part in recall procedures.

FDA.gov

Have you found that your medication is part of the recall? Here’s what you should do:

Consumers

If you find that your lot of medication is part of this recall, do the following:

1. Call your doctor right away. Ask for a new prescription to replace your recalled medication and report any changes in your symptoms.
2. Continue to monitor your health for any adverse symptoms over the next week and notify your physician if any concerns are noted.
3. Consumers should contact Inmar by telephone at 1-877-597-0878. They are available Mon-Fri from 9:00am to 5:00pm (EST). You can also contact them via email at rxrecalls@inmar.com.
4. If you are currently experiencing or have experienced an adverse reaction to this medication (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
5. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Inmar by telephone at 1-877-597-0878 or you can utilize rxrecalls@inmar.com to contact them via email. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Inmar by telephone at 1-877-597-0878 or you can utilize rxrecalls@inmar.com to contact them via email. Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled medication.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

Medical Waste Disposal Services

MedWaste’s Blog Index

Medical Waste Regulations

MedWaste’s Product Store

Learn How To Properly Manage & Dispose of Household Medical Waste

A voluntary national recall has been issued from Jarman’s Midwest Cleaning Systems, Inc. for their 75% and 80% Isopropyl Alcohol and Hand Sanitizer due to the possible presence of methanol. At the time of the writing of this notice, there have been no reports of adverse events, but the risk of major reactions including death remains high.

SUMMARY

Date of Recall:

Announced: March 27, 2023

Public Notification: March 28, 2023

Name(s) of Drug:

Midwest Cleaning Solutions, Clean Pro Supply

Isopropyl Alcohol Antiseptic 75% Topical Solution Hand Sanitizer, Non-Sterile Solution

Alcohol Antiseptic 80% Topical Solution Hand Sanitizer Non-Sterile Solution

Company Name:

Jarman’s Midwest Cleaning Systems, Inc.

Drug Indication:

Hand Sanitizer

Product Description

The sanitizer was distributed in gallon sized, clear or white plastic bottles. The bottles were sold individually and in 4-bottle cases.

Reason for Recall

At this time, no adverse reactions have been reported. However, exposure to Methanol through topical (skin), inhalation (breathing in fumes) or consumption (drinking the fluid) can lead to reactions such as:

• Nausea
• Vomiting
• Headache
• Dermatitis
• Blurred vision
• Loss of Appetite
• Abdominal Pain
• Gastrointestinal Bleeding
• Diarrhea
• Pancreatitis
• Giddiness
• Insomnia
• Mania
• Amnesia
• Visual Hallucinations
• Tachycardia (fast heart rate)
• Bradycardia (slow heart rate)
• Hypotension (low blood pressure)
• Tachypnea (fast breathing)
• Respiratory Arrest (no longer breathing)
• Seizures
• Blindness
• Permanent damage to the central nervous system
• Coma
• Death

Impacts

Consumers who have used or been exposed to the contaminated hand sanitizer may experience any of the previously listed symptoms immediately or up to 72 hours following exposure.

Lot information

Consumers can locate the DOM (date of manufacturing) and the NDC (national drug code) on bottles matching the volumes listed on the chart below.

FDA.gov

Have you found that your product is part of the recall? Here’s what you should do:

Consumers

If you find that your lot of sanitizers is part of this recall, do the following:

1. Call your doctor right away and notify them of any exposure that you have had to the drug.
2. Continue to monitor your health for any adverse symptoms over the next 72 hours and notify your physician if any concerns are noted.
3. Consumers should contact Jarman’s Midwest Cleaning systems, Inc at 1-800-288-0741 with questions or refund requests. They are available Mon-Fri from 8:30am to 5:00pm (CST). You can also contact them via email at recall@mwcleaningsolutions.com.
4. If you are currently experiencing or have experienced an adverse reaction to this drug (listed above), notify your physician immediately and notify the FDA by calling 1-800-332-1088 or completing an online reporting form.
5. Contact MedWaste Management for information and/or assistance with disposing of the recalled solution.

Retailer

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Jarman’s Midwest Cleaning systems, Inc at 1-800-288-0741 or you can utilize recall@mwcleaningsolutions.com to contact them via email. Notify them of any recalled batches that have already been sold to consumers.
3. Notify affected consumers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled solution.

Wholesaler

1. Examine all inventory and remove stock that is affected by the recall immediately.
2. Contact Jarman’s Midwest Cleaning systems, Inc at 1-800-288-0741 or you can utilize recall@mwcleaningsolutions.com to contact them via email.  Notify them of any recalled batches that have already been shipped to retailers.
3. Notify affected retailers of recalled batches that they have already or will receive.
4. Contact MedWaste Management for information and/or assistance with disposing of the recalled solution.

We are MedWaste Management – California’s medical waste disposal experts!

Established in 2008, MedWaste Management fills a need for compliant and safe medical waste disposal to the healthcare industry and the general public alike. We publish this blog in order to spread useful and practical information to help you stay safe, smart and healthy!

Call us with any questions or to start service at (866) 254-5105. We are always happy to help!

Check out our services and other great resources in the links below.

Medical Waste Disposal Services

MedWaste’s Blog Index

Medical Waste Regulations

MedWaste’s Product Store

Learn How To Properly Manage & Dispose of Household Medical Waste