CGMP Deviations; laboratory testing was not followed in accordance with GMP requirements
CGMP Deviations; laboratory testing was not followed in accordance with GMP requirements
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 Teva Pharmaceuticals USA to request your refund or repair — edit it as you like.
Subject: Recall D1292-2014 — Teva Pharmaceuticals USA Teva Pharmaceuticals USA recalls METHYLDOPA Tablets USP, 500 mg, 100 count Hello, I own a Teva Pharmaceuticals USA recalls METHYLDOPA Tablets USP, 500 mg, 100 count bottle, Rx only, Manufactured In INDIA By: EMCURE PHARMACEUTICALS LTD that is covered by recall D1292-2014 from Teva Pharmaceuticals USA. 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.
