Product Wiki · Recalls · Health Canada — Medical Devices

Durepair Dura Subsitute — recall 73891

Health Canada — Medical Devices · Canada · 2023-06-30 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
73891
Date of alert
2023-06-30
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Neurology
Product type
Medical devices
Reported risk: Medtronic was informed by the contract manufacturer that based on internal investigation they have identified issues with in-process and finished goods endotoxin testing. these issues may have resulted in the release of product with out-of-specification endotoxin levels. Recall start date: June 13, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/durepair-dura-subsitute

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