International safety notice

BRF/URF for cobas 8100 automated workflow series,

Swiss / SwissMedic · CHE · Mar 6, 2017

Key facts

Title BRF/URF for cobas 8100 automated workflow series,
Regulator Swiss / SwissMedic
Country CHE
Brand BRF/URF for cobas 8100 automated workflow series,
Manufacturer Hitachi High-Technologies
Models 02-xx, 03-01, 20-Feb-2017, SBN-CPS-2017-003, 07441657001, 07439954001
Event type Safety Notice
Date Mar 6, 2017
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice

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