Dlp Antegrade Aortic Root Cardioplegia Cannulae
Recall Summary DLP Antegrade Aortic Root Cardioplegia Cannulae have been recalled across Canada due to a performance issue. These are medical devices used during heart surgery to deliver cardioplegia solution to the aortic root. The recall is classified as Class I, indicating a serious potential health risk.
- Product
- DLP Antegrade Aortic Root Cardioplegia Cannulae
- Reason
- Performance
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2025-02-13
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/b55b0b99-d00f-4796-ab55-d464cb10ae59