Weck Efx Endo Facial Closure System
Weck EFX Endo Facial Closure System Recall Weck EFX Endo Facial Closure System devices are being recalled across Canada due to a manufacturing defect that could cause the device to malfunction during use. This is a Class I recall, the most serious classification. The recall affects all units of this surgical closure system that were distributed in Canada.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-12-05
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/551cd5f1-a8fd-4697-aeaa-8cc838b77a3c