Product Wiki · Recalls · Health Canada — Medical Devices

Patient Data Module — recall 25735

Health Canada — Medical Devices · Canada · 2011-12-09 · Type III

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Agency: Health Canada — Medical Devices
Recall identifier: 25735
Date of alert: 2011-12-09
Country / jurisdiction: Canada
Authority classification: Type III
Notice type: recall
Product category: Medical devices
Product type: Medical devices
Notice status: Archived by the issuing authority — kept for reference

Reported risk: When certain monitoring systems using a patient data module are configured for auto-mode non-invasive blood pressure measurements, it is possible that the auto-mode measurements may stop automatically cycling. The problem may not be apparent to the caregiver because the last measurement remains on the screen. The caregiver can, however, view the timestamp of the last auto-mode determination to see that periodic cycling has stopped.

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

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Patient Data Module — recall 25735

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