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Class II · ModerateRecall completed

Losartan Potassium

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot#: 7901903A, exp. date 04/2024
Where it was soldNationwide in the USA.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

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

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byVivimed Life Sciences Private Limited, Plot No. 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram- 603 110, Tamilnadu, India foreign manufacturer
Brand nameLOSARTAN POTASSIUM
Generic nameLOSARTAN POTASSIUM
Active ingredient(s)LOSARTAN POTASSIUM
Distributed by / forStrides Pharma Inc.
NDC64380-933-08
Show the full FDA record
Full product labelLosartan 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 firmStrides Pharma Inc.
DistributionNationwide in the USA.
Quantity2,700 HDPE Bottles
Recall initiated2023-06-26
Report date2023-07-12
Recall completed2024-05-15
Recall numberD-0895-2023
ClassificationClass II
FDA statusTerminated
Origin on fileEast Brunswick NJ United States

Related

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.