Product Wiki · Recalls · Health Canada — Medical Devices

JOURNEY Knee System — recall 61102

Health Canada — Medical Devices · Canada · 2018-07-05 · Type II

As described by Health Canada — Medical Devices: JOURNEY Knee System - Femoral OXINIUM and COCR Nonporous Bi-Cruciate Stabilized (BCS) (2018-06-19)

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Agency
Health Canada — Medical Devices
Recall identifier
61102
Date of alert
2018-07-05
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The analysis of available post-market surveillance data suggests that patients that have been implanted with a first generation JOURNEY BCS Knee System may have a higher risk of requiring a revision earlier than they or their surgeon had expected.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/journey-knee-system-femoral-ox

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