Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by: The Kroger Co, Cincinnati, OH 45202, Manufactured for: Torrent Pharma Inc., 150 Allen Road, Suite 102, Basking Ridge, NJ 07920, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045 NDC 68645-494-54
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lots: 180190, 180191 (exp 10/2020) and 181597 (exp 02/2021)
- 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:
- Legacy Pharmaceutical Packaging LLC
- Reason for Recall:
- CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) detected.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Losartan Potassium Tablets, USP, 50 mg, 30 tablet bottles, Rx Only, Distributed by: The Kroger Co, Cincinnati, OH 45202, Manufactured for: Torrent Pharma Inc., 150 Allen Road, Suite 102, Basking Ridge, NJ 07920, Packaged by: Legacy Pharmaceutical Packaging LLC, Earth City, MO 63045 NDC 68645-494-54
Product Codes/Lot Numbers:
Lots: 180190, 180191 (exp 10/2020) and 181597 (exp 02/2021)
Distribution:
Distributed in: AZ, IN, TN
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: D-1075-2019
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