Ultra Intra-aortic Balloon Pumps (iabp)
Recall Summary Ultra Intra-Aortic Balloon Pumps (IABP) are being recalled in Canada due to a performance issue. These devices are used to assist heart function in patients with severe heart conditions. The recall affects all units distributed across Canada.
- Product
- Ultra Intra-Aortic Balloon Pumps (IABP)
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-05-07
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/64f5d743-4097-4343-91b2-478b2ac2f6d1