Dxa 5000 (2020-06-16)
DxA 5000 Recall Summary The DxA 5000 medical device has been recalled across Canada due to safety or performance concerns classified as Class I, meaning there is a serious risk to health. The recall affects all DxA 5000 units distributed throughout Canada. This device falls under the drugs and medical devices category.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2020-06-26
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/9d908c87-55b6-4769-90b8-184b7586544c