Dxa 5000 (2021-07-21)

DXA 5000 Recall Summary The DXA 5000 medical device has been recalled across Canada due to a safety issue classified as Class I, the most serious type. The recall affects all DXA 5000 devices that were distributed throughout Canada.

Reason

Medical devices

Classification

Class I

Category

drug recall

Country

Canada

Agency

HC-DEVICES

Recall date

2021-08-06

Status

Ongoing

Distribution

Canada-wide

Official recall notice from HC-DEVICES

Recall details on Nibble Recalls: https://trynibble.app/recalls/07d9d398-c847-44ea-80eb-870f1e09a05a