Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-118-01
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lots# H03125, H03225, H03325, Exp Date: 2027/08
- 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:
- Leading Pharma, LLC
- Reason for Recall:
- CGMP Deviations; presence of N-nitroso-Furosemide (NNF) above the recommended intake limit.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Furosemide Tablets, USP, 80 mg, 100 Tablets bottles, Rx only, Manufactured by: Leading Pharma, LLC, Fairfield, NJ 07004, NDC 69315-118-01
Product Codes/Lot Numbers:
Lots# H03125, H03225, H03325, Exp Date: 2027/08
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-0486-2026
Related Recalls
Class I - Dangerous
Superpotent Drug: Assay value found to be 110.6% in Chlomipramine Hydrocholoride capsules
Class I - Dangerous
Labeling: Label Error on Declared Strength. Bottle labeled as 0.5 mg tablets contained 1mg tablets of lorazepam