Coaguchek Softclix Lancing Device
CoaguChek SofTclix Lancing Device Recall CoaguChek SofTclix lancing devices are being recalled across Canada because they may not operate properly, potentially causing them to fail to puncture the skin or to puncture incorrectly when used. This device is used by people who need to monitor their blood clotting levels. The recall affects all CoaguChek SofTclix lancing devices distributed in Canada.
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2016-09-07
- Status
- Closed
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/d51cfec9-479a-4455-aa7a-cc27df52f4fa