Medtronic Dlp Retrograde Cardioplegia Cannulae
Medtronic is recalling DLP Retrograde Cardioplegia Cannulae devices across Canada due to a sterility concern. These devices are used during heart surgery to deliver cardioplegia solution. The recall is classified as Class II, which indicates a situation where use of the product could result in serious adverse health consequences.
- Product
- Medtronic DLP Retrograde Cardioplegia Cannulae
- Reason
- Sterility concern
- Classification
- Class II
- Category
- medical device recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2026-04-30
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/3548afab-e09e-4796-9005-f38b644d4ed5