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Medtronic dlp retrograde cardioplegia cannulae
Official notice
30 Apr 2026
Last checked
30 Apr 2026
An official Health Canada notice concerns Medtronic dlp retrograde cardioplegia cannulae. On 8-January-2026, Medtronic received a complaint from the U.S. Reporting that a seal of a pouch containing the cannula was not fully sealed (chevron side) and opened to the air. The customer reported that they identified seventeen (17) cannulae with open pouches and therefore considered the product unsterile. There was no patient involvement in the complaint. Published 2026-04-30.
What to do now
Contact the manufacturer if you require additional information.
Recall number
82009
Official notice
2026-04-30
The hazard
The hazard
On 8-January-2026, Medtronic received a complaint from the U.S. Reporting that a seal of a pouch containing the cannula was not fully sealed (chevron side) and opened to the air. The customer reported that they identified seventeen (17) cannulae with open pouches and therefore considered the product unsterile. There was no patient involvement in the complaint.
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
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Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
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Brand: Medtronic.
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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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