Product Wiki · Recalls · Health Canada — Medical Devices

HistoCore PELORIS 3 (2018-05-16) — recall 60995

Health Canada — Medical Devices · Canada · 2018-06-01 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
60995
Date of alert
2018-06-01
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Health products
Product type
Medical devices
Reported risk: If operator initiates an operation in second retort or the protocol running concurrently in second retort causes a dialog box to appear when draining first retort at completion of protocol, a software defect may interrupt instrument workflow sequences in the first retort resulting in the impeller continuing to rotate.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/histocore-peloris-3-2018-05-16

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