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Health Canada Medical devices

DLP Vessel Cannulae

Issued February 22, 2024
Issue
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
Hazard description
Labelling and packaging
Product
Product name
DLP Vessel Cannulae
Reference
ID
RA-75117