Ultane recall
Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51
Why was Ultane recalled?
Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: 1088856, Exp 6/20
- Product
- Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51
- Recalling firm
- AbbVie Inc.
- Quantity
- 7,770 bottles
- Distribution
- MS, OH
- Recall date
- February 7, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)