Dx-d 600 (2016-05-02)
DX-D 600 Recall Summary The DX-D 600 medical device has been recalled across Canada due to a safety or effectiveness issue classified as Class I (the most serious type). The recall affects all DX-D 600 devices that were distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-05-16
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/2c778eb7-5d8b-44ac-8a81-f7f57c82ec7f