RecallHawk
Class II Recall

Losartan Potassium Tab. USP 50mg, Pkg Size: 30, Mfg: Lupin Pharmaceuticals, Inc., Preferred Pharmaceuticals, Inc.

Preferred Pharmaceuticals, Inc.

Summary

The FDA issued a Class II for Losartan Potassium Tab. USP 50mg, Pkg Size: 30, Mfg: Lupin Pharmaceuticals, Inc. by Preferred Pharmaceuticals, Inc.. Reason: CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits..

Details

Source

Drug Recall

External ID

D-0789-2022

Action Date

2022-05-04

Status

Terminated

Category

drug

Product Description

Losartan Potassium Tab. USP 50mg, Pkg Size: 30, Mfg: Lupin Pharmaceuticals, Inc., Preferred Pharmaceuticals, Inc.

Lot/Code Info: Lot: E1321O, Exp.: 5/31/2023 Lot: E2521H, Exp.: 5/31/2023 Lot: E2621F, Exp.: 5/31/2023

Quantity Affected: 44 Bottles of 90 Tablets 33 Bottles of 30 Tablets

Reason for Recall

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

Distribution

Nationwide within the U.S to CA, IN and FL.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-12

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 121 drug recalls issued in the same week, part of 267 drug-related FDA actions this month.

Preferred Pharmaceuticals, Inc. has 36 FDA actions in our database, including 36 recalls.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

What should I do if I have this product?

Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Preferred Pharmaceuticals, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Preferred Pharmaceuticals, Inc. have FDA actions?

Preferred Pharmaceuticals, Inc. has 36 FDA actions in our database, including 36 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "D-0789-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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