Health product recall

DLP™ Elongated One Piece Arterial Cannulae

Brand(s)
Last updated

Summary

Product
DLP™ Elongated One Piece Arterial 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™ Elongated One Piece Arterial Cannulae

2022041038
2023020934

77418
77422

Issue

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

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-76724

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