Cobas U Cuvette (400 Pc)

Cobas U Cuvette (400 Pc) Recall Summary Cobas U Cuvette products are being recalled across Canada due to performance issues. This recall affects a medical testing product used in laboratory settings. The recall is classified as Class I, indicating a serious concern related to how the product functions.

Product
Cobas U Cuvette (400 Pc)
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2024-11-14
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/b1b7b50f-dce8-4ea6-a17f-aaca43908a3e