Product Wiki · Recalls · Health Canada — Medical Devices

Philips Allura Xper and Azurion 7 Systems — recall 73951

Health Canada — Medical Devices · Canada · 2023-07-13 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
73951
Date of alert
2023-07-13
Country / jurisdiction
Canada
Authority classification
Type II
Notice type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: Philips has become aware of several situations that can result in a loss of availability of the wireless foot switch during a procedure. Identified issues that may result in the wireless foot switch not being available are: • Loss of bluetooth connection due to interferences from other radio equipment • Battery not fully charged • Battery not holding its charge • Damage in the charger, cable and/or connector of the wireless foot switch Recall start date: July 4, 2023
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/philips-allura-xper-and-azurio

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