Class II โ€” Potential Health Hazard

Potential health hazard โ€” use of or exposure to this product may cause temporary or medically reversible adverse health consequences.

Losartan Potassium Tab. USP 50mg Recalled by Preferred Pharmaceuticals, Inc Due to CGMP Deviations: FDA lab confirmed presence of an...

Date: April 30, 2019
Company: Preferred Pharmaceuticals, Inc
Status: Terminated
Source: FDA (Drug)

What You Should Do

Stop using this product immediately. Do not consume, use, or distribute it.

Return the product to the place of purchase for a full refund. If you have questions, contact Preferred Pharmaceuticals, Inc directly.

Affected Products

Losartan Potassium Tab. USP 50mg, a) 30 count bottle (NDC 68788-0048-03) and b) 90 count bottle (NDC 68788-0048-09), Rx only, Preferred Pharmaceuticals, Inc., Anaheim, CA, Mfg: Torrent Pharma Inc., Basking Ridge, NJ

Why Was This Recalled?

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer

Where Was This Sold?

This product was distributed to 4 states: CA, GA, IN, VA

Affected (4 states)Not affected

About Preferred Pharmaceuticals, Inc

Preferred Pharmaceuticals, Inc has 10 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report