Roche Diagnostics Gmbh Monitors And Near Patient Immunoassay Instrument (2016-01-06)

Roche Diagnostics GMBH is recalling certain monitors and near-patient immunoassay instruments distributed across Canada due to a medical device issue classified as Class I, which is the most serious type of recall. The specific defect or safety concern in these devices has not been detailed in this notice. This recall affects devices that were in distribution throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2016-01-22

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/ab3c1d08-d4f4-4beb-937f-a5a44b9f7423