Product Wiki · Recalls · Health Canada — Medical Devices

MobileDiagnost wDR, REL. 2 — recall 56500

Health Canada — Medical Devices · Canada · 2017-01-18 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
56500
Date of alert
2017-01-18
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Health products
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: When the operator connects the unit to the mains using a non-hospital-grade mains outlet, the protective earth connection may not be effective and an electrical defect inside the unit could cause a dangerous voltage to be present on the housing. The operator may not be aware of such danger, when the "Hospital grade mains connector required" warning label is missing, which must be present in Canada according to local electrical codes.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/mobilediagnost-wdr-rel-2

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