Dlp™ Elongated One Piece Arterial Cannulae
Recall Summary DLP™ Elongated One Piece Arterial Cannulae are being recalled across Canada due to labelling and packaging issues. This is a Class I recall, which is the most serious classification. The affected products are used as medical devices for arterial access during medical procedures.
- Product
- DLP™ Elongated One Piece Arterial Cannulae
- Reason
- Labelling and packaging
- Classification
- Class I
- Category
- drug recall
- Country
- Canada
- Agency
- HC-DEVICES
- Recall date
- 2024-12-19
- Status
- Ongoing
- Distribution
- Canada-wide
Official recall notice from HC-DEVICES
Recall details on Nibble Recalls: https://trynibble.app/recalls/8bf3cd0c-a892-4e3f-beb6-ef161c211a34