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

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Recall of Male Enhancement Capsules

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.

Product Package Size UPC Lot # Exp Date
Pro Power Knight Plus Capsule, 2550 mg 1-count 4 9492290522 0 N/A 06/2026
NUX Male Enhancement Capsule 1-count 6 0157751236 3 RO 927996 12/25/2024
DYNAMITE SUPER Capsule,

58,000 mg

1-count 6 7579937602 7 OMS760-B 12/2025

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.

 

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Tammy McKinney, RN, creator 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 reach out to her directly on LinkedIn!

 


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