Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202, UPC 343386-450-114, NDC 43386-450-11
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot#: S700065, Exp. 02/2019; 700619, Exp. 08/2019
- 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:
- LUPIN SOMERSET
- Reason for Recall:
- Subpotent Drug and Failed Content Uniformity.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Nitrofurantoin Oral Suspension USP, 25mg/5mL, 230 mL Bottle, Rx Only, Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202, UPC 343386-450-114, NDC 43386-450-11
Product Codes/Lot Numbers:
Lot#: S700065, Exp. 02/2019; 700619, Exp. 08/2019
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0927-2018
Related Recalls
Class I - Dangerous
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Class I - Dangerous
Failed Impurities/Degradation Specifications