Official recall record
Medtronic DLP Retrograde Cardioplegia Cannulae
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2026-05-01
- Last updated (per notice)
- 2026-04-30
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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