Product Wiki · Recalls · Health Canada — Medical Devices

Unicel DXH Slidemaker Stainer System (2014-02-06) — recall 51360

Health Canada — Medical Devices · Canada · 2014-03-21 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
51360
Date of alert
2014-03-21
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: If the "ordering physician" option is selected in the system manager label configuration screen, the Unicel DXH slide maker stainer coulter cellular analysis system will print the name of the primary physician instead of the ordering physician on the slide label. The ordering physician's name correctly transmits to the laboratory information system. the primary identifier, the date/time and other demographic information will appear as selected on the slide label. Slide making and staining quality are not affected.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/unicel-dxh-slidemaker-stainer-

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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