Product Wiki · Recalls · Health Canada — Medical Devices

Mobilediagnost WDR (2018-06-01) — recall 61046

Health Canada — Medical Devices · Canada · 2018-06-14 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
61046
Date of alert
2018-06-14
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Philips has become aware when the operator or a bystander touches the area of the inner part of the vertical sliding column (on which the tube arm moves up or down), without paying attention of the tube arm movement, the fingers can be pinched.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/mobilediagnost-wdr-2018-06-01

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