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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