🔍 RecallPedia

ExtenZe 600 mg, 30 tablet box, Manufactured for: Biotab Nutraceuticals, Inc., Pasadena, CA.

Class I - Dangerous
💊 Drugs Recalled: January 9, 2014 Schindele Enterprises Prescription Drugs

What Should You Do?

  1. Check if you have this product:
    Lot 0512058, Exp. 05/16
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Schindele Enterprises dba Midwest Wholesale
Reason for Recall:
Marketed Without an Approved NDA/ANDA: These dietary supplements contain undeclared sildenafil, an analogue of sildenafil, and/or tadalafil.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

ExtenZe 600 mg, 30 tablet box, Manufactured for: Biotab Nutraceuticals, Inc., Pasadena, CA.

Product Codes/Lot Numbers:

Lot 0512058, Exp. 05/16

Distribution:

Distributed in: PA, IL, TX, IA, GA, CT, FL, CA, LA, NY, MD, NV, WI

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: D-1339-2014

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