Product Wiki · Recalls · Health Canada — Medical Devices

MagNA Pure 24 Instrument (2018-10-13) — recall 58910

Health Canada — Medical Devices · Canada · 2018-11-30 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
58910
Date of alert
2018-11-30
Country / jurisdiction
Canada
Risk level
Type III
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: There is a potential for cross-contamination when using specific protocols (HGDNA 200 version 1, HGDNA DS 200 version 1, fast HGDNA 200 version 1 and HGDNA 1000 protocols version 2) on the MagNA Pure 24 System. A new version of the protocol set (version 1.4) is available. It includes updated versions of the HGDNA 200 (version 2.0), HGDNA ds 200 (version 2.0), fast HGDNA 200 (version 2.0) and HGDNA 1000 protocols (version 3.0). The protocols have been updated to exclude the risk of a potential cross-contamination without affecting the purification performance of the HGDNA protocols.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/magna-pure-24-instrument-2018-

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