Cobas P501 Post-analytical Units (2019-04-07)

Cobas p501 Post-Analytical Units Recall Roche Diagnostics is recalling cobas p501 post-analytical units distributed across Canada due to a defect in the medical device. The units are used in laboratory settings to process and handle test samples after analysis. This is a Class I recall, which is the most serious classification for medical devices.

Reason
Medical devices
Classification
Class I
Category
drug recall
Country
Canada
Agency
HC-DEVICES
Recall date
2019-04-18
Status
Ongoing
Distribution
Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/1860b08c-5a4a-476b-bcf7-675ae2dda18f