Product Wiki · Recalls · Health Canada — Medical Devices

MICROFUGE 20R 120 V 60 HZ WITH FA241.5P IVD (2016-03-08) — recall 54671

Health Canada — Medical Devices · Canada · 2016-03-29 · Type III

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Agency
Health Canada — Medical Devices
Recall identifier
54671
Date of alert
2016-03-29
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: Beckman Coulter has identified that the power boards on the affected units may have an incorrect component. As a result, the power board may short circuit resulting in an error code 22, which will cause the centrifuge to become inoperable.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/microfuge-20r-120-v-60-hz-fa24

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