Nationwide Recall of Male Enhancement Capsules Announced - MedWaste Management Nationwide Recall of Male Enhancement Capsules Announced - MedWaste Management

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Arize male enhancement supplement recall

Nationwide Recall of Male Enhancement Capsules Announced

In cooperation with the FDA, manufacturer Today the World announced a voluntary recall of all lots of their Arize herbal dietary supplement capsules. The capsules contain undeclared Nortadalafil, a substance not approved for use in this manner. Nortadalafil may interact with prescription medications, causing dangerous and life-threatening medical consequences.

As of the writing of this notice, no adverse events have yet been reported.

SUMMARY

 

Date of Recall:

Announced: February 2, 2024

Public Notification: February 5, 2024

Name(s) of Drug:

Arize Herbal Dietary Supplement

Company Name:

Today the World

Drug Indication:

Erectile Dysfunction

Arize packaging front FDA recall
Arize packaging back FDA recall

Product Description

Arize is marketed as a male enhancement supplement for the treatment of Erectile Dysfunction. The product was distributed via an online retailer at www.getarize.com. It was shipped in packs of 10 capsules in a black box bearing the name “Arize” in red with the tagline, “For a Rise That’s HARD to Forget.”

Reason for Recall

The FDA analyzed the capsules and found the presence of Nortadalafil, a substance that is neither declared on the packaging nor approved for use by the manufacturer.

Impacts

Consumers who ingest the supplement may experience an interaction between the Nortadalafil and their medication. This may lead to symptoms of hypotension (low blood pressure), including weakness, lightheadedness, fainting, confusion, blurred vision, nausea, vomiting, and even DEATH. Those who take the following medications are at highest 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

Recall Lot Information

The recall includes all lots of Arize. See below for instructions on taking part in recall procedures.

Product

Lot #

Exp Date

Arize

2107

10/2024

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. Monitor your health for adverse symptoms and notify your physician if you notice any changes.
  4. Consumers may request a full refund from where they purchased their product. They may also contact the manufacturer by telephone at 1-888-767-4889 or via email at info@getarize.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 assistance with disposing of the recalled supplement.

Retailer

  1. Examine all inventory and remove stock affected by the recall immediately.
  2. Contact the manufacturer by telephone at 1-888-767-4889 or info@getarize.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 assistance with disposing of the recalled supplement.

Wholesaler

  1. Examine all inventory and remove stock affected by the recall immediately.
  2. Contact the manufacturer by telephone at 1-888-767-4889 or via email at info@getarize.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 assistance with disposing of the recalled supplement.

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Tammy McKinney, Nurse Writer

Tammy McKinney, RN, founder of HelpfulHospiceNurse, is a healthcare writer and seasoned registered nurse. With experience in acute care, long-term care, rehabilitation, drug & alcohol, and hospice & palliative care, she combines her medical understanding with her love for writing to educate and inform the public on various health-related topics. You can view a snippet of her portfolio here or contact her directly on LinkedIn!

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