Official recall record
DLP Vessel Cannulae
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-02-22
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Medtronic received a complaint that while using the vessel cannula, the cannula type indicated on the pouch did not match the cannula type that was in the pouch. The pouch contained model 30001 (blunt tip) instead of model 30000 (beveled tip) . Recall start Date: February 7, 2024
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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