Centricity™ High Acuity Anesthesia

Recall Summary Centricity™ High Acuity Anesthesia products are being recalled across Canada due to a performance issue. This recall affects the anesthesia drug product distributed throughout Canada. The FDA has classified this as a Class I recall, indicating a serious concern.

Product
Centricity™ High Acuity Anesthesia
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-05-03
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/098fb085-19ad-4372-b4eb-3f7d8b99e83b