Intraclude Intra-aortic Occlusion Device (2018-04-02)
IntraClude Intra-aortic Occlusion Device Recall The IntraClude Intra-aortic Occlusion Device is being recalled across Canada. The device was found to have defects related to how it was manufactured or designed. This recall affects patients who have received or may receive this device for aortic occlusion procedures.
- Reason
- Medical devices
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2018-05-18
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/84ff47ae-054d-41a1-a4b2-5022ad6ef34d