PlainRecalls
FDA Drug Moderate Class II Terminated

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

Reported: April 10, 2019 Initiated: March 1, 2019 #D-1075-2019

Product 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

Reason for Recall

CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) detected.

Details

Units Affected
179,544 30-count bottles
Distribution
AZ, IN, TN
Location
Earth City, MO

Frequently Asked Questions

What product was recalled?
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. Recalled by Legacy Pharmaceutical Packaging LLC. Units affected: 179,544 30-count bottles.
Why was this product recalled?
CGMP Deviations: presence of an impurity, N-Methylnitrosobutyric acid (NMBA) detected.
Which agency issued this recall?
This recall was issued by the FDA Drug on April 10, 2019. Severity: Moderate. Recall number: D-1075-2019.