Vitek Ms (2013-10-07)

Vitek MS Recall Summary Vitek MS, a medical device, was recalled across Canada on October 7, 2013, due to unspecified safety or performance concerns classified as Class I (the most serious type). This recall affected medical device users and healthcare facilities across the country that had the Vitek MS system.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2013-11-25

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/d7ecc0da-fe55-4437-b11b-1a019ae31d90