Product Wiki · Recalls · Health Canada — Medical Devices

DELFIA/AutoDELFIA P1GF Kit (2019-08-07) — recall 59823

Health Canada — Medical Devices · Canada · 2019-08-16 · Type II

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Agency
Health Canada — Medical Devices
Recall identifier
59823
Date of alert
2019-08-16
Country / jurisdiction
Canada
Risk level
Type II
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Reported risk: Manufacturer has become aware that the measured PlGF analyte concentrations in patient samples may be decreased on average 50% due to a change in one of the raw materials.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/delfiaautodelfia-p1gf-kit-2019

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