International safety notice

Corrective Action for VITROS 5.1 FS System Software-Version 2.6.1 and below, VITROS 4600 Chemistry System Software Version 2.0 and below, VITROS 5600 Integrated System Software-Version 2.0 and below, Ortho-Clinical Diagnostics

Germany / BfArM · DEU · Jul 17, 2012

Key facts

Title Corrective Action for VITROS 5.1 FS System Software-Version 2.6.1 and below, VITROS 4600 Chemistry System Software Version 2.0 and below, VITROS 5600 Integrated System Software-Version 2.0 and below, Ortho-Clinical Diagnostics
Regulator Germany / BfArM
Country DEU
Brand VITROS 5.1 FS System Software-Version 2.6.1 and below, VITROS 4600 Chemistry System Software Version 2.0 and below, VITROS 5600 Integrated System Software-Version 2.0 and below, Ortho-Clinical Diagnostics
Manufacturer Corrective Action for VITROS 5.1 FS System Software-Version 2.6.1 and below, VITROS 4600 Chemistry System Software Version 2.0 and below, VITROS 5600 Integrated System Software-Version 2.0 and below, Ortho-Clinical Diagnostics
Models CL12-154_EU, 2.6.1, CL12-173_EU, PV2-097
Date Jul 17, 2012
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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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

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