Public Alert No: 0013/2019 – Recall Of Beast Capsules By Stiff Boy LLC
July 11, 2019,
The National Agency for Food and Drug Administration and Control has been informed by the United States Food and Drug Administration that (US FDA) that STIFF BOY LLC is voluntarily recalling Beast capsules due to presence of undeclared Sildenafil.
Sildenafil is a drug used for the treatment of male erectile dysfunction and is in a class of drugs called phosphodiesterase (PDE-5) inhibitors.
Consumption of a product with undeclared PDE-5 inhibitors may pose a threat to consumers because the active ingredients may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may lower blood pressure to dangerous levels which can be life threatening.
Product Name: Beast Capsules
Manufacturers name: STIFF BOY LLC, USA.
Product description: The Blue fusion capsule is a dietary supplement for male sexual enhancement and is packaged in blue wrapping and a blue box with a picture of a beast on it.
NAFDAC implores all importers, wholesalers and retailers to immediately stop the importation, distribution and sale of the affected beast capsules.
Health care providers and members of the public are also advised to stop the administration and use of the affected products to avoid negative health implications. Healthcare providers and anyone in possession of the affected products should submit them to the nearest NAFDAC office.
Consumers are advised to report adverse events related to the use on any of these products to the nearest NAFDAC office, NAFDAC PRASCOR (20543 TOLL FREE from all networks) or via email@example.com
NAFDAC: Customer-focused, Agency-minded!!!