Vitros® Versatips And Vitros® Microtips

Recall Summary Ortho Clinical Diagnostics is recalling Vitros® Versatips and Vitros® Microtips products across Canada due to performance issues. These are medical testing supplies used in laboratory settings. The FDA has classified this as a Class I recall, which is the most serious category.

Product
Vitros® Versatips and Vitros® Microtips
Reason
Performance
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2023-08-25
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/771e27c5-4634-4c32-ac8e-48d1932bbc1b