CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.
CGMP Deviations: An FDA inspection identified inadequate investigations of past market complaints.
We break every recall down into plain English — this one’s still on our list. Until our write-up is ready, the official FDA hazard and remedy below have the full, accurate details.
We’ve drafted a message you can send Wockhardt Usa Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1346-2015 — Wockhardt Usa Inc. Wockhardt Usa Inc. recalls Lisinopril Tablets USP, 5 mg, 1000-count bottles, Rx Hello, I own a Wockhardt Usa Inc. recalls Lisinopril Tablets USP, 5 mg, 1000-count bottles, Rx Only, Manufactured by: Wockhardt Limited, Mumbai, India; that is covered by recall D-1346-2015 from Wockhardt Usa Inc.. 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.
