Product Wiki · Recalls · Health Canada — Medical Devices

Patient Data Module (PDM) (2020-05-21) — recall 61355

Health Canada — Medical Devices · Canada · 2020-06-12 · Type II

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Agency: Health Canada — Medical Devices
Recall identifier: 61355
Date of alert: 2020-06-12
Country / jurisdiction: Canada
Risk level: Type II
Risk type: recall
Product category: Medical devices
Product type: Medical devices

Reported risk: While using Carescape PDM, the accompanying monitor may display incorrect ECG data if pace detection is turned on and an AED is used to perform defibrillation.

Primary source: https://recalls-rappels.canada.ca/en/alert-recall/patient-data-module-pdm-2020-0

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Patient Data Module (PDM) (2020-05-21) — recall 61355

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