Intraclude Intra-aortic Occlusion Device (2019-01-21)
IntraClude Intra-Aortic Occlusion Device Recall The IntraClude Intra-Aortic Occlusion Device is being recalled across Canada due to a Class I safety issue. This device is used in medical procedures to temporarily block blood flow in the aorta. The recall affects all units of this device that were distributed in Canada.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-03-08
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/78479afc-fcaf-4311-b049-4b3ef0c60117