International safety notice

Corrective action for the VITROS® 3600 Immunodiagnostic Systems, VITROS® 4600 Chemistry Systems and VITROS® 5600 Integrated Systems, Ortho Clinical Diagnostics (OCD)

Germany / BfArM · DEU · Oct 28, 2014

Key facts

Title Corrective action for the VITROS® 3600 Immunodiagnostic Systems, VITROS® 4600 Chemistry Systems and VITROS® 5600 Integrated Systems, Ortho Clinical Diagnostics (OCD)
Regulator Germany / BfArM
Country DEU
Brand the VITROS® 3600 Immunodiagnostic Systems, VITROS® 4600 Chemistry Systems and VITROS® 5600 Integrated Systems, Ortho Clinical Diagnostics (OCD)
Manufacturer Corrective action for the VITROS® 3600 Immunodiagnostic Systems, VITROS® 4600 Chemistry Systems and VITROS® 5600 Integrated Systems, Ortho Clinical Diagnostics (OCD)
Models PY1‐075, 2014-191_EU, XX‐JULY‐2014, 6802413, 6802445, WITH‐191, CL2014, 6802783
Date Oct 28, 2014
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 1–9 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