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Health & beauty Canada Health product recall

DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae

Medtronic DLP Select 3D Arterial Cannula and DLP Elongated One Piece Arterial Cannulae are affected; they can be identified by model/catalogue numbers 78222, 78322, 77422, 77522, 77622 and 77722 and specific lot/serial numbers including 0232612916, 0232602300 and 0232745036 (elongated cannulae have more than 10 lot/serial numbers; contact manufacturer). The recall was issued after complaints beginning in April 2026 of pinhole leaks in the wire‑wound body of 22 Fr EOPA™ elongated one piece and EOPA 3D™ arterial cannulae used during cardiopulmonary bypass. Contact the manufacturer for additional information.

What's being recalled

Companies: Medtronic Inc., 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432.

How to identify it

Affected products: DLP Select 3D Arterial Cannula; Lot or serial number: 0232612916; Model or catalogue number: 78222

Affected products: DLP Select 3D Arterial Cannula; Lot or serial number: 0232602300; Model or catalogue number: 78222

Affected products: DLP Select 3D Arterial Cannula; Lot or serial number: 0232745036; Model or catalogue number: 78322

Affected products: DLP Elongated One Piece Arterial Cannulae; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 77722

Affected products: DLP Elongated One Piece Arterial Cannulae; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 77422

Affected products: DLP Elongated One Piece Arterial Cannulae; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 77522

Affected products: DLP Elongated One Piece Arterial Cannulae; Lot or serial number: More than 10 numbers, contact manufacturer.; Model or catalogue number: 77622

The hazard

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.

What to do

Contact the manufacturer if you require additional information.

The official notice

This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.

Read the official notice (opens in a new tab)

A little guidance

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