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Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted July 01, 2022
Male Enhancement Supplements Sold on Amazon Recalled
On January 27, 2022, Loud Muscle Science LLC issued a voluntary recall of various lots of Launch Sequence supplements because they were found to contain the prescription drug Tadalfil.
Tadalafil (the active ingredient in Cialis) is an ingredient in FDA approved products in the family of drugs known as phosphodiesterase (PDE-5) inhibitors and is prescribed for erectile dysfunction. These drugs can cause symptoms like headache and flushing and can interact with medications containing nitrates such as nitroglycerine, resulting in dangerously low blood pressure.
Recalled Launch Sequence supplements (see product images) are marketed as dietary supplements for male sexual enhancement. They were sold nationwide in the USA and Canada on Amazon, eBay.com, and retail stores and can be identified by the following:
- Launch Sequence Capsules, 60 count in bottle, ASIN: B07TLPWXDS and B08HM7VHCX, UPC: 641378938375 and 661020848166. Lot Numbers: C07172101, 2022054, 2021001, and 2022104.
- Launch Sequence Euphoria Capsules, 10 count in tin, ASIN: B08ZJX4V9J, UPC: 661020846864. Lot Numbers: C07172101, 2022054, 2021001, and 2022104.
- Launch Sequence Aphrodisia Capsules, 4 count in tin, ASIN: B07QB3S2LV and B09S12VK3F, UPC: 661020846957. Lot Numbers: C07172101, 2022054, 2021001, and 2022104.
Consumers who have the recalled supplements should discontinue use and discard.
Consumers and healthcare providers can report any adverse reactions to the FDA's FDA's MedWatch Voluntary Reporting Program.
See ConsumerLab’s Review of Sexual Enhancement Supplements for more information and tests of related products.
For more information, use the link below.
See related recalls and warnings:
Sexual Enhancement Capsules for Men Recalled
Three Sexual Enhancement Supplements Sold on Amazon Recalled
NS NY Distributor Inc Male Enhancement Products Recalled Due to Undeclared Drugs
Three More Male Enhancement Products Recalled Due to Undeclared Drugs
Three Male Enhancement Products Recalled Due to Undeclared Drugs
Report a Problem
If you have experienced an unexpected and adverse reaction to a dietary supplement, nutritional product, or generic drug, we would like to hear about it, as we may investigate the problem. Please select from one of these options:
Dietary Supplement or Nutritional Product Problem Report
If you believe that a dietary supplement (e.g., vitamin, mineral, or herbal supplement) or other nutritional product has caused an unexpected, adverse reaction, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their Safety Reporting Portal at https://www.safetyreporting.hhs.gov.
Please complete the form below as accurately as possible. You may need to check the label on the product.
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Generic Drug Problem Report
If you believe that a generic drug has not acted like the original drug, we would like to know about it. We are collecting and organizing this information and may publish it. We might test the product in the future. You may also want to report the problem to the U.S. FDA through their MedWatch program at the FDA MedWatch website.
Please complete the form below as accurately as possible. You may need to check the label on the drug.
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