Product Wiki · Recalls · Health Canada — Medical Devices

McKesson Cardiology Hemo (2019-03-22) — recall 59485

Health Canada — Medical Devices · Canada · 2019-04-05 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
59485
Date of alert
2019-04-05
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Users are not notified of procedure medication discrepancies between the vitals and meds, the procedure notes and patient common data screens in McKesson Cardiology Hemo.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/mckesson-cardiology-hemo-2019-

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