AbbVie Inc. recalls Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, US…
- Recall date
- January 22, 2018
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0412-2018
- FDA classification
- Class III
- Brand / firm
- AbbVie Inc.
- Sold / distributed
- MS, OH
Why it was recalled
Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51
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