Product Wiki · Recalls · Health Canada — Medical Devices

Duradiagnost — recall 56624

Health Canada — Medical Devices · Canada · 2017-06-13 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 56624
Date of alert: 2017-06-13
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: Philips discovered that some welding joints on the vertical carriage brackets of the tube stand may crack. As a result, the tube arm assembly may exhibit uncharacteristic sideways movement, with the tube becoming off center. If all of the welding joints cracked, the tube arm assembly could fall down.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/duradiagnost

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Duradiagnost — recall 56624

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