DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae
Brand(s)
Last updated
Summary
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
Affected 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.
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies
| Medtronic Inc. |
| 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432 |
Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Recall date
Identification number
RA-82278
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