Schindele Enterprises recalls Sexy Monkey 2000mg dietary supplements due to undeclared sildenafil and tadalafil. These unapproved ingredients pose health risks. Consumers should check product details and contact the company for guidance.
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Schindele Enterprises recalls Sexy Monkey 2000mg dietary supplements because they contain undeclared sildenafil and tadalafil without proper FDA approval. This poses health risks as these substances are not approved for use in dietary supplements.
These supplements contain undeclared sildenafil and tadalafil, which are prescription drugs. Without FDA approval, they can cause serious health issues like heart problems or interactions with other medications.
Anyone who purchased or uses Sexy Monkey 2000mg dietary supplements from the distributor. People with underlying health conditions or those taking other medications may be at higher risk.
Check for the product name 'Sexy Monkey', 2000 mg, 1 count blister, distributed by A Herbal Bio, Inc., Bayside, NY. The product has no lot number and expires December 31, 2014.
Look for the product name 'Sexy Monkey', 2000 mg, 1 count blister, distributed by A Herbal Bio, Inc., Bayside, NY with no lot number and expiration date December 31, 2014.
The product contains undeclared sildenafil and tadalafil without FDA approval, which can cause serious health risks.
The recall record does not specify a remedy, so contact Schindele Enterprises for guidance.
The recall states the product contains undeclared prescription drugs, which can cause health issues, but the exact risk level is not specified.
We’ve drafted a message you can send Schindele Enterprises to request your refund or repair — edit it as you like.
Subject: Recall D-1336-2014 — Schindele Enterprises Schindele Enterprises Hello, I own a Schindele Enterprises that is covered by recall D-1336-2014 from Schindele Enterprises. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
