Official recall record
DLP™ Elongated One Piece Arterial Cannulae
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-12-19
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
During the manufacturing process of the seven specified lot numbers, products for the models were incorrectly labeled with an incorrect size. Based on complaints received, Medtronic cannot determine the exact number of mislabeled units, but it is confirmed that at least one cannula from each of the listed lot numbers has been mislabeled. Recall start date: December 12, 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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