AbbVie Inc. recalls Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only
See all recalls from AbbVie Inc. →Recalled Product
Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51
Hazard / Issue
Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.
Issued by
FDA
Affected States: MS, OH
Lot/Code Info: Lot #: 1088856, Exp 6/20
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
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Search Amazon for Ultane (sevoflurane), 250 mL, →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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