Failed Stability Specifications: product may not meet specification limit for assay test.
Failed Stability Specifications: product may not meet specification limit for assay test.
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 Apotex Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-1814-2015 — Apotex Inc. Apotex Inc. recalls Cevimeline Hydrochloride Capsules, 30 mg a) 100 count bottle, and b Hello, I own a Apotex Inc. recalls Cevimeline Hydrochloride Capsules, 30 mg a) 100 count bottle, and b) 500 count bottle, Rx Only, Manufactured by: Apotex that is covered by recall D-1814-2015 from Apotex 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.
