Dx-d 600 (2018-08-15)

Recall Summary The DX-D 600 device has been recalled across Canada due to a medical device issue. This recall is classified as Class I, indicating a serious safety concern. The device was distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2018-08-31

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/747e66df-55b5-4de1-8048-36bca4693e5f