Recalls & Warnings
ConsumerLab.com is keeping you informed with current product recalls and warnings.
Posted April 03, 2024
ForeverMen Sexual Enhancement Supplements Recalled Due to Undeclared Prescription Drugs
On February 12, 2024, ForeverMen issued a recall of all lots of ForeverMen capsules, which are promoted for sexual enhancement, after FDA analysis found the capsules to contain undeclared sildenafil and tadalafil.
Sildenafil (the active ingredient in Viagra) and tadalafil (the active ingredient in Cialis) are 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 ForeverMen capsules were distributed nationwide and are packaged in a blister card within a 10-count box. The company is notifying consumers of the recall through the recall announcement below.
Consumers who purchased the recalled products should immediately discontinue use of the product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these drug products.
Consumers and healthcare providers can report any adverse reactions to the FDA's MedWatch Voluntary Reporting Program.
See ConsumerLab.com's Review of Sexual Enhancement Supplements for more information and tests of related products.
For more information, use the link below.
ForeverMen Supplements Recalled
See related recalls and warnings:
Eleven Brands of Sexual Enhancement Supplements Recalled Due to Undeclared Prescription Drugs
Sustain and Schwinnng Male Enhancement Supplements Recalled
FDA Warns Amazon for Selling Men’s Supplements Containing Prescription Drugs
Total Body Nutrition, TBN Labs, and Loud Muscle Science Banned from Selling Adulterated and Misbranded Dietary Supplements
Pain Relief Tea Recalled, Found to Contain Prescription Drugs
Sildenafil (the active ingredient in Viagra) and tadalafil (the active ingredient in Cialis) are 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 ForeverMen capsules were distributed nationwide and are packaged in a blister card within a 10-count box. The company is notifying consumers of the recall through the recall announcement below.
Consumers who purchased the recalled products should immediately discontinue use of the product. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using these drug products.
Consumers and healthcare providers can report any adverse reactions to the FDA's MedWatch Voluntary Reporting Program.
See ConsumerLab.com's Review of Sexual Enhancement Supplements for more information and tests of related products.
For more information, use the link below.
ForeverMen Supplements Recalled
See related recalls and warnings:
Eleven Brands of Sexual Enhancement Supplements Recalled Due to Undeclared Prescription Drugs
Sustain and Schwinnng Male Enhancement Supplements Recalled
FDA Warns Amazon for Selling Men’s Supplements Containing Prescription Drugs
Total Body Nutrition, TBN Labs, and Loud Muscle Science Banned from Selling Adulterated and Misbranded Dietary Supplements
Pain Relief Tea Recalled, Found to Contain Prescription Drugs