Product Wiki · Recalls · Health Canada — Medical Devices

McKesson Cardiology Hemo (2020-01-03) — recall 63079

Health Canada — Medical Devices · Canada · 2020-01-20 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
63079
Date of alert
2020-01-20
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Change Healthcare has identified an issue where for procedures performed in calendar year 2020, when editing procedure notes or charting free text notes in the McKesson Cardiology Hemo procedure log, the note's date/time stamp may change to an incorrect date/time stamp.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/mckesson-cardiology-hemo-2020-

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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