Health product recall

DLP Vessel Cannulae

Brand(s)
Last updated

Summary

Product
DLP Vessel Cannulae
Issue
Medical devices - Labelling and packaging
What to do

Contact the manufacturer if you require additional information. 

Audience
Healthcare

Affected products

Affected products

Lot or serial number

Model or catalog number

DLP Vessel Cannulae

2023020890

30000

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

Additional information

Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Companies

Medtronic Inc.

710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432

Published by
Health Canada
Audience
Healthcare
Recall class
Type II
Identification number
RA-75117

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