Strides Pharma Inc. recalls Losartan Potassium 100mg tablets (Rx only) manufactured by Vivimed Life Sciences in India due to AZIDO impurity levels exceeding safety limits. Affected lots have specific expiration dates and NDC codes.
CGMP Deviations- AZIDO Impurity levels observed to be above acceptable limits
Strides Pharma Inc. is recalling Losartan Potassium 100mg tablets (Rx only) because they contain AZIDO impurities at levels above acceptable safety limits. This could pose a health risk if taken by patients.
The recall is due to AZIDO impurities found in the medication that exceed acceptable safety limits. This could potentially cause health issues if the medication is taken as directed.
Patients prescribed Losartan Potassium 100mg tablets by a doctor are affected. Those who have the specific lots with listed expiration dates and NDC codes are most at risk.
Check the product label for the NDC code 64380-935-05 or 64380-935-08. Look for the specific lots listed with their expiration dates (e.g., Lots 7901047B through 7901302B expiring through January 2023).
Discontinue use of the recalled Losartan Potassium 100mg tablets if you have them.
The medication contains AZIDO impurities at levels above acceptable safety limits, which could pose a health risk.
Affected lots include specific NDC codes (64380-935-05 and 64380-935-08) with expiration dates from May 2022 through January 2023.
Check the product label for the NDC code 64380-935-05 or 64380-935-08 and verify the lot numbers listed with their expiration dates.
We’ve drafted a message you can send Strides Pharma to request your refund or repair — edit it as you like.
Subject: Recall D-0974-2022 — Strides Pharma Strides Pharma Hello, I own a Strides Pharma that is covered by recall D-0974-2022 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.
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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.
