Labeling: Incorrect or Missing Package Insert: Package insert is missing warning regarding anaphylaxis.
Labeling: Incorrect or Missing Package Insert: Package insert is missing warning regarding anaphylaxis.
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 Valeant Pharmaceuticals North America LLC to request your refund or repair — edit it as you like.
Subject: Recall D-1059-2016 — Valeant Pharmaceuticals North America LLC Valeant Pharmaceuticals North America LLC recalls SECONAL Hello, I own a Valeant Pharmaceuticals North America LLC recalls SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant that is covered by recall D-1059-2016 from Valeant Pharmaceuticals North America 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.
