Product Wiki · Recalls · Health Canada — Medical Devices

UniMatch Plus Software (2019-01-31) — recall 58731

Health Canada — Medical Devices · Canada · 2019-02-15 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
58731
Date of alert
2019-02-15
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: The UniMatch Plus Software that uses lot specific software catalog files (CHR_005_201807v1.uch) contain incorrect specificity information for lane 63, which may result in an ambiguous result or a mistyping. The impacted software catalog files were released and available for use between the date period Oct 12 2018 and Nov 15, 2018. Only files analyzed during this period are impacted. Worksheets for the accessory product are correct.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/unimatch-plus-software-2019-01

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.