Recall MonitorHealth Products
DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae
· Published by Health Canada · Official notice
Details
Alert type: Health product recall
Category: Health products - Medical devices - Cardiovascular
Product: DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae
Issue: Medical devices - Performance, Medical devices - Sterility
What to do: Contact the manufacturer if you require additional information.
Audience: Healthcare
Recall class: Type II
Products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| DLP Select 3D Arterial Cannula | 0232612916 | 78222 |
| DLP Select 3D Arterial Cannula | 0232602300 | 78222 |
| DLP Select 3D Arterial Cannula | 0232745036 | 78322 |
| DLP Elongated One Piece Arterial Cannulae | More than 10 numbers, contact manufacturer. | 77722 |
| DLP Elongated One Piece Arterial Cannulae | More than 10 numbers, contact manufacturer. | 77422 |
| DLP Elongated One Piece Arterial Cannulae | More than 10 numbers, contact manufacturer. | 77522 |
| DLP Elongated One Piece Arterial Cannulae | More than 10 numbers, contact manufacturer. | 77622 |
Issue
Beginning in April 2026, complaints were received regarding pinhole leaks in the wire-wound body of 22 Fr EOPA™ elongated one piece arterial cannulae and EOPA 3D™ arterial cannulae used during cardiopulmonary bypass procedures.