Intraclude Intra-aortic Occlusion Device (2019-05-22)
IntraClude Intra-aortic Occlusion Device Recall The IntraClude Intra-aortic Occlusion Device is being recalled across Canada due to safety concerns with the medical device itself. This recall is classified as Class I, the most serious category. The device was distributed throughout Canada and may affect patients who received this implant.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2019-07-16
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b6dd7da9-5106-4cf3-932f-64770e365a62