Dvantx Legacy System And Precision 500d System (2017-02-09)

Recall Summary Advantx Legacy System and Precision 500D System devices are being recalled across Canada due to a medical device issue. This recall is classified as Class I, meaning there is a serious potential health risk associated with these products. The devices were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2017-02-28

Status

Closed

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/9ea7eeeb-9d4a-4634-b4cb-142b8af2fd0f