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Dlp select 3d arterial cannula and dlp elongated one piece arterial cannulae
Official notice
3 Jul 2026
An official Health Canada notice concerns Dlp select 3d arterial cannula and dlp elongated one piece arterial cannulae. 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. Published 2026-07-03.
What to do now
Contact the manufacturer if you require additional information.
Recall number
82278
Official notice
2026-07-03
The hazard
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.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
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Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
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Company & contacts
Company & contacts
Brand: Medtronic.
Source & status
Source & status
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Recall details
Recall details
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Documents, notices & source
See the official notice and source documents for full details.
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