Bd Veritor Plus Analyzer (2019-03-31)

BD Veritor Plus Analyzer Recall Summary The BD Veritor Plus Analyzer, a medical testing device, has been recalled across Canada due to safety or performance concerns. This is classified as a Class I recall, which is the most serious type. The recall affects all units of this device that were distributed throughout Canada.

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/3ae72683-ae54-4124-8fda-3c2fac8caac2