Product Wiki · Recalls · Health Canada — Medical Devices

DIMENSION VISTA LOCI ESTRADIOL (2016-01-14) — recall 55019

Health Canada — Medical Devices · Canada · 2016-01-25 · Type I

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Agency
Health Canada — Medical Devices
Recall identifier
55019
Date of alert
2016-01-25
Country / jurisdiction
Canada
Risk level
Type I
Risk type
recall
Product category
Medical devices
Product type
Medical devices
Notice status
Archived by the issuing authority — kept for reference
Reported risk: Siemens Healthcare Diagnostics is conducting a correction for all lots of ADVIA Centaur Enhanced Estradiol, Dimension Vista LOCI Estradiol, IMMULITE/IMMULITE 1000 Estradiol and IMMULITE 2000 Estradiol. Siemens has confirmed the drug fulvestrant (FASLODEX) may cause falsely elevated estradiol results in the assays listed.
Primary source: https://recalls-rappels.canada.ca/en/alert-recall/dimension-vista-loci-estradiol

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