Reported Jun 8, 2022 · Terminated
Losartan Potassium Tablets, USP, 50 mg, Rx Only, Manufactured by: Vivimed Life Sciences Private Limited, Plot No., 101,…
Strides Pharma Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Strides Pharma Inc. · 2 Tower Center Blvd Ste 1102 · East Brunswick, NJ · 08816-1100
Is this the product you have?
- Losartan Potassium Tablets, USP, 50 mg, Rx Only
- Manufactured byVivimed Life Sciences Private Limited, Plot No., 101, 102, 107 & 108, SIDCO Pharmaceutical Complex, Alathur, Kanchipuram - 603 110, Tamilnadu, India
- Distributed byStrides Pharma Inc., East Brunswick, NJ 08816. 90 film coated tablets NDC 64380-934-05 1000 film coated tablets NDC 64380-934-08
- Lot codes and dates
7 of 7 products
Products covered by this recall # Product as published 1 Lot 7901146A, 7901147A, 7901148A & 7901149A, Exp Date Sep-22 2 Lot 7901279A, 7901280A, 7901281A, 7901282A, 7901283A & 7901284A, Exp Date Nov-22 3 Lot 7901359A, 7901360A & 7901361A, Exp Date Dec-22 4 Lot 7901362A, 7901406A, 7901407A, 7901408A & 7901409A, Exp Date Jan-23. 64380-934-08 5 Lot 7901008A & 7901009A, Exp Date Jun-22 6 Lot 7901150A & 7901151A, Exp Date Sep-22 7 Lot 7901285B, 7901286B, 7901287A, 7901288A, 7901289A, 7901290A, 7901291A, 7901292A, 7901293A & 7901294A, Exp Date Nov-22. - Amount recalled
- 381456 bottles
This recall covers 3 products
The agency filed one notice per product. You are reading one of them; the other 2 are below.
Where it was sold
- Nationwide
Why it was recalled
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
This product could cause temporary or reversible health problems — stop using it.
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