May 7, 2024

Dietary Supplements Recalled for Undeclared Drugs

R. Thomas Marketing LLC, in conjunction with Just Enhance LLC,  is voluntarily recalling all lots of dietary supplements because they contain Sildenafil, a PDE-5 inhibitor that is the active ingredient in an FDA-approved drug for erectile dysfunction, making them tainted and unapproved drugs. Sildenafil is not listed on product labels. This ingredient poses a threat to consumers because Sildenafil may interact with nitrates found in some prescription drugs and can lower blood pressure to dangerous levels. There is no word on whether or not any adverse reactions have been reported to date. You can see the long list of recalled products at the FDA web site, along with product sizes. They include Black Ant, Herb Viagra, Real Skill, Stree Overlord, Weekend Prince, and African Black Ant. … [Read more...]

APEXXX and OPAL Tablets Recalled for Undeclared Sildenafil

Nuway Distributors is voluntarily recalling all lots of APEXXX tablets, because they contain sildenafil, a PDE-5 inhibitor, making this supplement an unapproved new drug. Sildenafil, an FDA-approved drug for erectile dysfunction, may interact with nitrates found in some prescription drugs and can lower blood pressure to life-threatening levels. The product may also cause headaches and flushing. This product is marketed as a dietary supplement for male sexual enhancement. It is packaged in a single blister pack containing 1 tablet. The UPC number is 705105963617. All lots of APEXXX sold in 2014 to June 2015 are included in this recall. APEXXX can be identified by black packaging. The yellow diamond shaped tablet is embossed with "APEXXX". It was sold in retail stores in Orlando, Florida … [Read more...]

Pink Bikini Dietary Supplement Recalled for Unapproved Drug

Lucy's Weight Loss System is voluntarily recalling all lots of Pink Bikini White powder Capsules because it tested positive for diclofenac after FDA sampling. This is a non steroidal anti-inflammatory drug (NSAID), which can increase the risk of fatal heart attack or stroke if you take high doses of it or take it long term, or if you have heart disease. If pregnant women take this drug during the last three months of pregnancy, it can harm the fetus. That makes this supplement an unapproved new drug. No reports of adverse events have been received to date. The product is packaged in clear bottles with white powder capsules. Each bottle has 30 capsules with 750 mg per capsule. The expiration date of the recalled product is 7/30/2017. It was distributed nationwide via … [Read more...]

Report Your Food Poisoning Case

Error: Contact form not found.

×
×

Home About Site Map Contact Us Sponsored by Pritzker Hageman, P.A., a Minneapolis, MN law firm that helps food poisoning victims nationally.