International safety notice
Information regarding VITROS® 5600 Integrated System because of a software anomaly, Ortho Clinical Diagnostics
Germany / BfArM · DEU · Jun 23, 2009
Key facts
| Title | Information regarding VITROS® 5600 Integrated System because of a software anomaly, Ortho Clinical Diagnostics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Information regarding VITROS® 5600 Integrated System because of a software anomaly, Ortho Clinical Diagnostics |
| Manufacturer | Information regarding VITROS® 5600 Integrated System because of a software anomaly, Ortho Clinical Diagnostics |
| Models | 1.2.4, CL09-194, SYJ-004 |
| Date | Jun 23, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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