International safety notice

RapidLab 1200 System

Swiss / SwissMedic · CHE · Dec 4, 2012

Key facts

Title RapidLab 1200 System
Regulator Swiss / SwissMedic
Country CHE
Brand RapidLab 1200 System
Manufacturer Siemens Healthcare Diagnostics Inc.
Models 10591, 29105, 914-631-8000, 1350036305, 12-70, 1335866035, 13-002, CH-8047, 5293926, 1350471681, POC-13-002
Event type Safety Notice
Date Dec 4, 2012
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