Labeling: Incorrect Package Insert; product packaged with outdated version of the insert
Labeling: Incorrect Package Insert; product packaged with outdated version of the insert
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 AbbVie Inc. to request your refund or repair — edit it as you like.
Subject: Recall D-901-2013 — AbbVie Inc. AbbVie Inc. recalls Mavik¿ trandolapril tablets 4mg, 100 count bottle, Rx only, Manufact Hello, I own a AbbVie Inc. recalls Mavik¿ trandolapril tablets 4mg, 100 count bottle, Rx only, Manufactured by Halo Pharmaceutical Inc., Whippany, NJ for that is covered by recall D-901-2013 from AbbVie 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.
