Strides Pharma recalls 25mg Losartan Potassium Tablets due to small blue plastic piece in some tablets. Rx-only medication sold in India with specific lot number.
Presence of Foreign Substance: Presence of a small piece of blue plastic embedded in the tablet.
Strides Pharma is recalling 25mg Losartan Potassium Tablets that may contain a small blue plastic piece. This foreign substance could cause injury if swallowed. The recall affects prescription-only medication sold in India with specific lot numbers.
A small piece of blue plastic can be embedded in the tablet. If swallowed, it could cause choking or internal injury. However, the risk is low because the plastic piece is small and the tablets are prescription-only.
Prescription-only Losartan tablets sold in India with lot number 7901903A (expiring April 2024) are affected. People taking this medication for high blood pressure are most at risk.
Check for the product name 'Losartan Potassium Tablets, USP, 25 mg' on the bottle. Look for the lot number 7901903A on the label. The tablets were sold in India with an expiration date of April 2024.
Inspect the tablet for a small blue plastic piece before taking it.
The product may contain a small blue plastic piece that could cause injury if swallowed. Do not take the tablet if you see plastic.
Check for a blue plastic piece. If present, do not take it. Contact your doctor for advice.
Look for the lot number 7901903A on the label. The product was sold in India with an expiration date of April 2024.
We’ve drafted a message you can send Strides Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0895-2023 — Strides Pharma Strides Pharma Hello, I own a Strides Pharma that is covered by recall D-0895-2023 from Strides Pharma. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.