Vitek® 2 Ast-n391

Recall Summary Vitek® 2 Ast-N391 is being recalled across Canada due to labelling and packaging issues. This product is used for antibiotic susceptibility testing in laboratory settings. The recall is classified as Class I, indicating a serious potential health risk.

Product
Vitek® 2 Ast-N391
Reason
Labelling and packaging
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2022-08-02
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/05b506d5-3ecb-4c1a-80ea-2dcfe8e56cb5