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An official Health Canada notice concerns Dlp cardiac vents & sumps. Since March 2024, there has been an increase in complaints reported for the DLP malleable left heart vent catheter for the catheters resisting shape retention when being bent. The catheters are intended to be malleable and retain a bend in the shaft. It was determined that the primary supplier updated their specification to remove annealing process to attain tensile strength listed in ASTM1313-18. Published 2025-09-24.
What to do now
Contact the manufacturer if you require additional information.
Recall number
78123
Official notice
2025-09-24
The hazard
The hazard
Since March 2024, there has been an increase in complaints reported for the DLP malleable left heart vent catheter for the catheters resisting shape retention when being bent. The catheters are intended to be malleable and retain a bend in the shaft. It was determined that the primary supplier updated their specification to remove annealing process to attain tensile strength listed in ASTM1313-18.
How to check if you're affected
How to check if you're affected
Compare the product name and identifiers below with the item you own. Follow the official notice if they match.
Recall Numbers
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Affected products
Product 1
Product 2
Product 3
Risk / hazard
Where it was sold
Where it was sold
The source does not list specific retailers. See the official notice for where affected products were sold.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand: Medtronic, Dlp Cardiac Vents Sumps.
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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