Liquiband Fix8 Open Hernia Mesh Fixation Device
Liquiband Fix8 Open Hernia Mesh Fixation Device is being recalled across Canada due to a manufacturing defect. This device is used during hernia repair surgery to secure mesh in place. The recall affects all units of this product distributed in Canada.
- Product
- Liquiband Fix8 Open Hernia Mesh Fixation Device
- Reason
- Manufacturing defect
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2022-02-14
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/5573febe-b921-43ff-ad77-5df741c90e7e