Medtronic Cannulae Products
Brand(s)
Summary
Contact the manufacturer if you require additional information.
Affected products
Affected products |
Lot or serial number |
Model or catalogue number |
|---|---|---|
Dlp Elongated One Piece Arterial Cannulae |
2023041365 |
77524 |
Clearview Blower/Mister |
2023040203 |
22120 |
Dlp Arteriotomy Cannulae |
2023041316 |
31001 |
Perfusion Adapter With Male Luer |
2023041227 |
25010 |
Dlp Cardiac Vents & Sumps |
2023041183 |
12010 |
Dlp Wirewound Curved Tip Arterial Cannula |
2023031282 |
87220 |
Dlp Single Stage Venous Return Cannulae |
More than 10 numbers, contact manufacturer. |
67318 |
Dlp One Piece Pediatric Arterial Cannula |
2023041343 |
77112 |
Dlp Oval Mc2 Two-Stage Venous Cannulae |
2023040116 |
91263C |
Dlp Pressure Display Set, Disposable |
2023030432 |
62000 |
Clearview Intravascular Arteriotomy Shunt |
2023041455 |
31125 |
Dlp Select Series Arterial Cannulae |
202305C184 |
72120 |
Dlp Antegrade Aortic Root Cardioplegia Cannulae |
202305C076 |
11014L |
Dlp Mc2 Two Stage Venous Cannula |
2023041071 |
91240C |
Cardiac Suction Tubes |
2023040913 |
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
| Medtronic Inc. |
| 710 Medtronic Parkway N.E., Minneapolis, Minnesota, United States, 55432 |
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