Flexible Shaft, Medullary (2016-05-19)
Recall Summary Flexible shaft medullary devices distributed across Canada are being recalled due to issues with the medical device itself. This recall is classified as Class I, the most serious type. The recall affects all patients and healthcare facilities in Canada that received these devices.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-05-31
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b99c3362-c248-4456-8ccf-536742de05fa