Famotidine Tablets USP, 20 mg, 100 count bottles, Rx Only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A. NDC 0378-3020-01
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot: 3018952, Exp 08/12
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- 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:
- Mylan Pharmaceuticals Inc.
- Reason for Recall:
- Impurities/Degradation Products: Out of specification results for Related Compound during routine stability testing.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx Only, Mylan Pharmaceuticals, Inc., Morgantown, WV 26505 U.S.A. NDC 0378-3020-01
Product Codes/Lot Numbers:
Lot: 3018952, Exp 08/12
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-1703-2012
Related Recalls
Prasugrel Tablets, USP, 5 mg, 30-count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc., Morgantown, WV 26505 U.S.A., NDC 0378-5185-93
MYLAN PHARMACEUTICALS
Class I - Dangerous
Failed Dissolution Specifications - low dissolution results
Class I - Dangerous
Labeling: Missing label: Label missing from some prefilled pens.
Class I - Dangerous
Labeling: Missing label on the vial