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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