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Medtronic dlp retrograde cardioplegia cannulae
Official notice
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 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
The source does not list specific retailers. See the official notice for where affected products were sold.
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Company & contacts
Brand: Medtronic.
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Documents, notices & source
See the official notice and source documents for full details.
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