Vitek 2 Compact 30 System - Instrument (2017-03-02)

VITEK 2 Compact 30 System Recall Summary The VITEK 2 Compact 30 System, a medical device used for microbial identification and testing, is being recalled across Canada. The recall was issued on March 2, 2017, and is classified as Class I, indicating a serious issue. The specific reason for the recall relates to concerns with the device itself, though detailed technical reasons are not specified in this notice.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-04-03

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/c0f399be-5e9f-4b16-b7fc-64f1ae553365