US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jun 26, 2023 (3 years ago)

Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only…

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

Why it was recalled

Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.

What was recalled

Losartan Potassium Tablets, USP, 25 mg, 1000 film coated tablets per bottle, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram- 603 110, Tamilnadu, India, NDC 64380-933-08

Recalling firm
Strides Pharma Inc.
NDC code
64380-933-08
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0895-2023

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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