Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51
Reported: February 7, 2018 Initiated: January 22, 2018 #D-0412-2018
Product Description
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.
Details
- Recalling Firm
- AbbVie Inc.
- Units Affected
- 7,770 bottles
- Distribution
- MS, OH
- Location
- North Chicago, IL
Frequently Asked Questions
What product was recalled? ▼
Ultane (sevoflurane), 250 mL, Inhalation Anesthetic, Rx only, Manufactured by: AbbVie Inc., North Chicago, IL 60064, USA. NDC 0074-4456-51. Recalled by AbbVie Inc.. Units affected: 7,770 bottles.
Why was this product recalled? ▼
Defective container: presence of a hole in the liners of the caps covering the product bottle, introducing possibility of leakage.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on February 7, 2018. Severity: Low. Recall number: D-0412-2018.
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