Medtronic Cannulae Products
Brand(s)
Last updated
Summary
Product
Medtronic Cannulae Products
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 Elongated One Piece Arterial Cannulae | 2023041365 2023040971 | 77524 77622 |
| Clearview Blower/Mister | 2023040203 2023040473 | 22120 |
| Dlp Arteriotomy Cannulae | 2023041316 2023041320 202305C146 2023041318 2023041318 2023041320 2023041318 2023041320 2023041318 2023041318 | 31001 |
| Perfusion Adapter With Male Luer | 2023041227 | 25010 |
| Dlp Cardiac Vents & Sumps | 2023041183 2023040819 2023040820 2023041184 | 12010 12008 |
| Dlp Wirewound Curved Tip Arterial Cannula | 2023031282 2023031283 | 87220 |
| Dlp Single Stage Venous Return Cannulae | More than 10 numbers, contact manufacturer. | 67318 67526 66128 67316 67528 68124 68130 67522 68134 68128 69320 66236 |
| Dlp One Piece Pediatric Arterial Cannula | 2023041343 | 77112 |
| Dlp Oval Mc2 Two-Stage Venous Cannulae | 2023040116 | 91263C |
| Dlp Pressure Display Set, Disposable | 2023030432 2023030736 2023030223 202305C225 2023031580 | 62000 61000 |
| Clearview Intravascular Arteriotomy Shunt | 2023041455 | 31125 |
| Dlp Select Series Arterial Cannulae | 202305C184 | 72120 |
| Dlp Antegrade Aortic Root Cardioplegia Cannulae | 202305C076 202306C138 | 11014L |
| Dlp Mc2 Two Stage Venous Cannula | 2023041071 2023041089 2023041088 2023041087 202306C074 2023041090 2023041084 | 91240C 91229C 91246C 91246 |
| Cardiac Suction Tubes | 2023040913 202305C057 | 10061 |
Issue
Medtronic is initiating a voluntary recall of units from specific lots of cannula products due to potential sterility breach.
Recall start date: March 19, 2024
Additional information
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Medical devices - Cardiovascular
Health products - Medical devices - General hospital and personal use
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-75325
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