Home/Recalls/CANADA-60006
Health CanadaType III

IMMULITE, 1000 and 2000 System- Progesterone Assay (2019-07-12)

Published: July 26, 2019Recall ID: 60006Category: generalCountry: Canada

Reason for Recall / Hazard

Medical devices

Product Description & Identification

IMMULITE, 1000 and 2000 System- Progesterone Assay (2019-07-12)

Additional Source Details

FieldValue
N I D60006
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/immulite-1000-and-2000-system-progesterone-assay-2019-07-12
IssueMedical devices
Title IMMULITE, 1000 and 2000 System- Progesterone Assay (2019-07-12)
Archived0
CategoryMedical devices
Last updated2019-07-26
OrganizationMedical devices
Recall classType III

Overview

  • Recalling FirmMedical devices
  • Risk LevelType III
Official Agency Alert