Synthes Flex Arm (2018-03-21)
Synthes Flex Arm Recall Summary Synthes Flex Arm devices are being recalled due to a defect that could affect their safe operation during medical procedures. The recall applies to devices distributed across Canada. This is classified as a Class I recall, which indicates a serious safety concern.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-05-01
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/bec3568e-5c4f-4711-a612-c88bc2e8a6df