Cardiosave Hybrid Iabp (2018-09-26)
Cardiosave Hybrid IABP Recall Summary The Cardiosave Hybrid IABP (intra-aortic balloon pump), a heart support device, has been recalled across Canada due to a medical device issue. This is a Class I recall, the most serious classification. 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
- 2018-11-02
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/374f1bc2-54ec-45d8-9977-83c8f48d6ceb