US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 8, 2019 (7 years ago)

Losartan Potassium USP, 50 mg, RX Only, Pkg By PD-Rx Pharmaceuticals Incorporated…

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

Why it was recalled

CGMP deviation: Product found to contain trace amounts of NMBA

What was recalled

Losartan Potassium USP, 50 mg, RX Only, Pkg By PD-Rx Pharmaceuticals Incorporated Oklahoma City, OK 73127 a) 60 Tablets NDC: 43063-854-60; b) 90 Tablets NDC: 43063-0854-90

Recalling firm
PD-Rx Pharmaceuticals, Inc.
Origin
OK, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0341-2021

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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