Product Wiki · Recalls · Health Canada — Medical Devices

CombiDiagnost R90 — recall 74402

Health Canada — Medical Devices · Canada · 2023-10-10 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
74402
Date of alert
2023-10-10
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Radiology
Product type
Medical devices
Reported risk: If the CombiDiagnost R90 System has a damaged wire in the System Power Distribution Unit (SPDU) within the m-cabinet and is connected to the ground, or the system experiences a power surge, there is the potential for a short circuit of the Electromagnetic Interference (EMI) filter or UA/UB board. If this issue occurs, the user may experience one or more of the following: - electrical fire within the main-cabinet (m-cabinet) - see or smell smoke - hear a popping sound coming from the m-cabinet Recall start date: October 28, 2021
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/combidiagnost-r90

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.