International safety notice

IMMULITE/IMMULITE 1000 Estradiol

Swiss / SwissMedic · CHE · Feb 24, 2020

Key facts

Title IMMULITE/IMMULITE 1000 Estradiol
Regulator Swiss / SwissMedic
Country CHE
Brand IMMULITE/IMMULITE 1000 Estradiol
Manufacturer Siemens Healthcare Diagnostics Products Limited
Models 01-6297401, 20-01.B.OUS, LKE21, 10381177, 05.01.2021, 10591, L2KE22, 1038117810381177, 10381132, 01.A.OUS, IMC20-01.B.OUS, L2KE26 and 5 more
Event type Safety Notice
Date Feb 24, 2020
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 10–99 Matching catalog numbers in FDA data

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About International device safety notices

Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.

Source: National medical device regulators (as listed), compiled by Orca1

Browse all International device safety notices