Product Wiki · Recalls · Health Canada — Medical Devices

Allura Xper FD10/10 — recall 58183

Health Canada — Medical Devices · Canada · 2018-08-02 · Type II

As described by Health Canada — Medical Devices: Allura Xper FD10/10 - Main Unit, Allura Xper FD10, Allura Xper FD20 - Main Unit and Allura Xper FD20/10 System - Main Unit (2018-07-17)

Compiled from an official source — the facts on this page are reproduced from the issuing authority’s own published notice, which is linked above. No AI-generated text appears on this page. How we use AI →
Agency
Health Canada — Medical Devices
Recall identifier
58183
Date of alert
2018-08-02
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: An incident has been reported to Philips in which the Monitor Ceiling Suspension (MCS), holding a FlexVision large screen 56-inch monitor, detached from the actuator rotor shaft. This caused the monitor to fall to the ground. When a monitor ceiling suspension detaches from the actuator rotor shaft and the monitor falls, there is a risk of injury for the patient, user and bystander.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/allura-xper-fd1010-main-unit-a

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