Medtronic Cannulae Products recall in Canada: sterility issue
In plain language
This recall involves various Medtronic Cannulae Products sold in Canada. They are being recalled due to a potential sterility breach. Stop using the product and contact the manufacturer for more information.
What to do
- Stop using the product immediately.
- Contact Medtronic Inc. if you require additional information.
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Affected products
Dlp Elongated One Piece Arterial Cannulae
Model: 77524, 77622
Lot: 2023041365, 2023040971
Clearview Blower/Mister
Model: 22120
Lot: 2023040203, 2023040473
Dlp Arteriotomy Cannulae
Model: 31001
Lot: 2023041316, 2023041320, 202305C146, 2023041318
Perfusion Adapter With Male Luer
Model: 25010
Lot: 2023041227
Dlp Cardiac Vents & Sumps
Model: 12008, 12010
Lot: 2023041183, 2023040819, 2023040820, 2023041184
Dlp Wirewound Curved Tip Arterial Cannula
Model: 87220
Lot: 2023031282, 2023031283
Dlp Single Stage Venous Return Cannulae
Model: 66128, 66236, 67316, 67318, 67522, 67526, 67528, 68124, 68128, 68130, 68134, 69320
Lot: More than 10 numbers, contact manufacturer.
Dlp One Piece Pediatric Arterial Cannula
Model: 77112
Lot: 2023041343
Dlp Oval Mc2 Two-Stage Venous Cannulae
Model: 91263C
Lot: 2023040116
Dlp Pressure Display Set, Disposable
Model: 61000, 62000
Lot: 2023030432, 2023030736, 2023030223, 202305C225, 2023031580
Clearview Intravascular Arteriotomy Shunt
Model: 31125
Lot: 2023041455
Dlp Select Series Arterial Cannulae
Model: 72120
Lot: 202305C184
Dlp Antegrade Aortic Root Cardioplegia Cannulae
Model: 11014L
Lot: 202305C076, 202306C138
Dlp Mc2 Two Stage Venous Cannula
Model: 91229C, 91240C, 91246, 91246C
Lot: 2023041071, 2023041089, 2023041088, 2023041087, 202306C074, 2023041090, 2023041084
Cardiac Suction Tubes
Model: 10061
Lot: 2023040913, 202305C057
Why this matters
Sterility issue
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: 2023030432, 2023030736, 2023030223, 202305C225, 2023031580, 2023031282, 2023031283, 2023040116, 2023040203, 2023040473, 2023040913, 202305C057, 2023041071, 2023041089, 2023041088, 2023041087, 202306C074, 2023041090, 2023041084, 2023041183, 2023040819, 2023040820, 2023041184, 2023041227, 2023041316, 2023041320, 202305C146, 2023041318, 2023041343, 2023041365, 2023040971, 2023041455, 202305C076, 202306C138, 202305C184, More than 10 numbers, contact manufacturer.
- 3
Check the model number
Model numbers are typically on the product label or packaging.
Affected models: 10061, 11014L, 12008, 12010, 22120, 25010, 31001, 31125, 61000, 62000, 66128, 66236, 67316, 67318, 67522, 67526, 67528, 68124, 68128, 68130, 68134, 69320, 72120, 77112, 77524, 77622, 87220, 91229C, 91240C, 91246, 91246C, 91263C
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Sterility issue
What should consumers do?
Stop using the product immediately. Contact Medtronic Inc. if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Sterility issue
When was this product recalled?
This product was recalled on April 3, 2024.
Is the MEDTRONIC INC. brand affected by this recall?
Yes, MEDTRONIC INC. products are affected by this recall. This recall involves various Medtronic Cannulae Products sold in Canada. They are being recalled due to a potential sterility breach. Stop using the product and contact the manufacturer for more information.