International safety notice
Corrective Action for ADVIA Centaur and ADVIA Centaur XP Multi Diluent 1, Siemens
Germany / BfArM · DEU · Aug 21, 2012
Key facts
| Title | Corrective Action for ADVIA Centaur and ADVIA Centaur XP Multi Diluent 1, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ADVIA Centaur and ADVIA Centaur XP Multi Diluent 1, Siemens |
| Manufacturer | Corrective Action for ADVIA Centaur and ADVIA Centaur XP Multi Diluent 1, Siemens |
| Models | 76432, 77075, 102.0, 103.0, 10813387, 78264, 83647, 77542, 78696, 02816138, 110312, 84123 and 35 more |
| Date | Aug 21, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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