Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.
Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.
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-0412-2018 — AbbVie Inc. AbbVie Inc. recalls Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manuf Hello, I own a AbbVie Inc. recalls Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, that is covered by recall D-0412-2018 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.
