Schindele Enterprises dba Midwest Wholesale recalls ExtenZe 600mg tablets due to undeclared sildenafil and tadalafil. This dietary supplement may contain unsafe levels of these drugs without FDA approval.
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Midwest Wholesale recalls ExtenZe 600mg tablets because they contain undeclared sildenafil and tadalafil without FDA approval. This poses a risk of unintended drug effects since these substances are prescription medications.
These dietary supplements contain undeclared sildenafil and tadalafil, which are prescription drugs. Without FDA approval, they may cause unintended side effects like heart problems or interactions with other medications.
People who purchased ExtenZe 600mg tablets from retailers like Midwest Wholesale are affected. Those with heart conditions or taking other medications are at higher risk due to potential interactions.
Check for ExtenZe 600mg tablets in 30-count boxes manufactured for Biotab Nutraceuticals, Inc. in Pasadena, CA. Lot number 0512058 with expiration 05/16.
Look for ExtenZe 600mg tablets in 30-count boxes with lot number 0512058 and expiration 05/16.
The tablets contain undeclared sildenafil and tadalafil without FDA approval, which can cause unintended side effects.
The recall record does not specify a remedy, so contact Midwest Wholesale directly for guidance.
Yes, people with heart conditions or taking other medications are at higher risk due to potential interactions.
We’ve drafted a message you can send Midwest Wholesale to request your refund or repair — edit it as you like.
Subject: Recall D-1339-2014 — Midwest Wholesale Midwest Wholesale Hello, I own a Midwest Wholesale that is covered by recall D-1339-2014 from Midwest Wholesale. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
