Failed Impurity/Degradation Specification; high out of specification for CAD II degradant
Failed Impurity/Degradation Specification; high out of specification for CAD II degradant
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 Corp. to request your refund or repair — edit it as you like.
Subject: Recall D-1570-2014 — Apotex Corp. Apotex Corp. recalls Candesartan Cilexetil and Hydrochlorothiazide Tablets 32 mg/12.5 Hello, I own a Apotex Corp. recalls Candesartan Cilexetil and Hydrochlorothiazide Tablets 32 mg/12.5 mg, 90 count bottles, Rx only, Manufactured by: Apotex that is covered by recall D-1570-2014 from Apotex Corp.. 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.
