Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits.
Failed Dissolution Specification: One lot of product did not meet the first stage dissolution specification limits.
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 D1834-2015 — Apotex Inc. Apotex Inc. recalls Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-c Hello, I own a Apotex Inc. recalls Verapamil Hydrochloride Extended-Release tablets, USP, 240 mg, 500-count bottles, Rx Only, Apotex Corp. Manufactured by that is covered by recall D1834-2015 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.
