Physiomesh Flexible Composite Mesh (2016-05-25)
PHYSIOMESH Flexible Composite Mesh Recall Summary Physiomesh Flexible Composite Mesh, a surgical implant used in hernia repair, has been recalled across Canada due to safety concerns with the medical device. The recall is classified as Class I, indicating a serious issue with the product. The device was distributed throughout Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-06-13
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/42270562-a957-44be-9517-af12d17fa605