Health product recall

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

Get notified

Receive notifications for new and updated recalls and alerts by category.

Subscribe