Official recall record
DLP Antegrade Aortic Root Cardioplegia Cannulae
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-02-13
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
During the manufacturing process, unexpected loose plastic material in the male luer used in the aortic root cannula was identified. The potential harms when identified prior to use is procedure delay while another cannula is located. If this is not identified prior to use, and the clinician uses the cannula, the potential harm is stroke (reversible and irreversible). Recall Start Date: February 5, 2025
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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