Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51

FDA recall notice · announced February 7, 2018 · Abbvie

Class III FDA/FSIS Class III: use is not likely to cause adverse health consequences.

The product

Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51

Reason for recall

Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.

Notes

Distribution: MS, OH
Lot/code information: Lot #: 1088856, Exp 6/20
Quantity: 7,770 bottles
Status: Terminated
Products in this recall event:
- Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51 (D-0412-2018)

Source: U.S. Food and Drug Administration public recall data. This page reports official records and is not legal, medical, or repair advice.