Health Canada3 Jul 2026
DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae
Health Canada published a recall notice for DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae on 3 Jul 2026. It is one of 311 notices of this kind from Health Canada since 2 Apr 2026 in AreaZine's record.
Recall
The recall notice
- Issued by
- Health Canada
- Issued
- 3 Jul 2026
- Recall type
- Health product recall
- Companies
- Medtronic Inc.710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432
- Official source
- Health Canada: the notice at its source
The latest from Health CanadaEvery warning and recall in Canada
Source: Health Canada: the notice at its source. AreaZine rebuilds this page from the agency's record; the agency's page is the one to act on. Contains information licensed under the Open Government Licence – Canada.
The notice as issued
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: 2026-07-03 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
Source: Health Canada: the notice at its source. The text is the agency's, unedited. Contains information licensed under the Open Government Licence – Canada.