Cobas It Middleware

Cobas IT Middleware Recall Summary Roche Diagnostics is recalling Cobas IT Middleware software used in laboratory diagnostic systems across Canada due to a potential malfunction that could affect the accuracy of test results. The recall applies to all Cobas IT Middleware versions currently in distribution. This is classified as a Class I recall, the most serious category, because the issue could result in incorrect medical test outcomes.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2017-03-10
Status
Closed
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/580923ac-3c08-455f-8d34-3555ac252b22