Tuftex® Embolectomy And Pruitt® Occlusion Catheters
Recall Summary TufTex® Embolectomy and Pruitt® Occlusion Catheters are being recalled in Canada because they may not be sterile. These are medical devices used in vascular procedures. The recall affects all units distributed throughout Canada.
- Product
- TufTex® Embolectomy and Pruitt® Occlusion Catheters
- Reason
- Sterility
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-04-29
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/eee79659-890c-4823-bc93-fc521ac20cd1