US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 6, 2022 (4 years ago)

Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles, Rx Only, Marketed and…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits

What was recalled

Losartan Potassium Tablets, USP 100 mg, 90 Tablets bottles, Rx Only, Marketed and Packaged By: PD-Rx Pharmaceuticals, Inc. Oklahoma City, OK 73127 Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108 SIDCO Pharmaceutical Complex, Alathur, Kanchipuram-603 110, Tamilnadu, India NDC 72789-165-90 UPC 3 72789 16590 5

Recalling firm
PD-Rx Pharmaceuticals, Inc.
NDC code
72789-165-90
Origin
OK, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1163-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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