Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
LOSARTAN POTASSIUM TABLETS USP Recalled by Micro Labs Usa, Inc S Due to Failed Content Uniformity Specifications; Dry mix failed blend...
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 Micro Labs Usa, Inc S directly.
Affected Products
LOSARTAN POTASSIUM TABLETS USP, 25 mg, 1000 Tablet Bottles, Rx Only. Manufactured by: Micro Labs Limited, Goa-403 722, INDIA. Manufactured for: Micro Labs USA, Inc., Princeton, NJ 08540. NDC 42571-110-10
Quantity: 144 bottles
Why Was This Recalled?
Failed Content Uniformity Specifications; Dry mix failed blend uniformity.
Where Was This Sold?
U.S. Including: New York
About Micro Labs Usa, Inc S
Micro Labs Usa, Inc S has 6 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report