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Dlp™ elongated one piece arterial cannulae
Official notice
19 Dec 2024
Last checked
19 Dec 2024
An official Health Canada notice concerns Dlp™ elongated one piece arterial cannulae. During the manufacturing process of the seven specified lot numbers, products for the models were incorrectly labeled with an incorrect size. Based on complaints received, Medtronic cannot determine the exact number of mislabeled units, but it is confirmed that at least one cannula from each of the listed lot numbers has been mislabeled. Recall start date: December 12, 2024 Published 2024-12-19.
What to do now
Contact the manufacturer if you require additional information.
Recall number
76724
Official notice
2024-12-19
The hazard
The hazard
During the manufacturing process of the seven specified lot numbers, products for the models were incorrectly labeled with an incorrect size. Based on complaints received, Medtronic cannot determine the exact number of mislabeled units, but it is confirmed that at least one cannula from each of the listed lot numbers has been mislabeled. Recall start date: December 12, 2024
How to check if you're affected
How to check if you're affected
Compare the VIN on your vehicle against the official list. If your VIN is listed, follow the official notice.
Recall Numbers
Lots
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Affected products
Product 1
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected vehicles were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand
Manufacturer
Phone
Brand: Medtronic, Dlp™ Elongated One Piece Arterial Cannulae.
Source & status
Source & status
Source
Tier
Category
Classification
App estimate
Recall details
Recall details
Recall number
Classification
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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