Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.
Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown 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 Actavis Mid Atlantic LLC to request your refund or repair — edit it as you like.
Subject: Recall D-006-2013 — Actavis Mid Atlantic LLC Actavis Mid Atlantic LLC recalls Prometh VC with Codeine Cough Syrup, CV, E Hello, I own a Actavis Mid Atlantic LLC recalls Prometh VC with Codeine Cough Syrup, CV, Each 5mL contains: Codeine phosphate 10mg; promethazine hydrochloride 6.25mg; that is covered by recall D-006-2013 from Actavis Mid Atlantic LLC. 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.
