Medtronic DLP Retrograde Cardioplegia Cannulae
Brand(s)
Last updated
Summary
Product
Medtronic DLP Retrograde Cardioplegia Cannulae
Issue
Medical devices - Sterility
What to do
Contact the manufacturer if you require additional information.
Audience
Healthcare
Affected products
| Affected products | Lot or serial number | Model or catalogue number |
|---|---|---|
| DLP Retrograde Cardioplegia Cannulae | 0231757975 | 94113T |
| DLP Retrograde Cardioplegia Cannulae | 0231667046 | 94113T |
| DLP Retrograde Cardioplegia Cannulae | 0231651336 | 94113T |
Issue
On 8-January-2026, Medtronic received a complaint from the U.S. reporting that a seal of a pouch containing the cannula was not fully sealed (chevron side) and opened to the air. The customer reported that they identified seventeen (17) cannulae with open pouches and therefore considered the product unsterile. There was no patient involvement in the complaint.
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
Recall date
Identification number
RA-82009
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