International safety notice
Corrective action for VITROS® 4600 Chemistry Systems & VITROS® 5600 Integrated Systems Software Version 3.0 and below, Ortho Clinical Diagnostics
Germany / BfArM · DEU · Oct 13, 2014
Key facts
| Title | Corrective action for VITROS® 4600 Chemistry Systems & VITROS® 5600 Integrated Systems Software Version 3.0 and below, Ortho Clinical Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | VITROS® 4600 Chemistry Systems & VITROS® 5600 Integrated Systems Software Version 3.0 and below, Ortho Clinical Diagnostics |
| Manufacturer | Corrective action for VITROS® 4600 Chemistry Systems & VITROS® 5600 Integrated Systems Software Version 3.0 and below, Ortho Clinical Diagnostics |
| Models | VITROS®‐232_EU, 2014-232_EU, 6802445, 6802413, CL2014‐232_LIST, XX‐SEPT‐2014, CALIBRATION1, CL2014WITH |
| Date | Oct 13, 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