International safety notice
Corrective Action for ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP, Siemens
Germany / BfArM · DEU · Nov 26, 2012
Key facts
| Title | Corrective Action for ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP, Siemens |
| Manufacturer | Corrective Action for ADVIA Centaur, ADVIA Centaur XP and ADVIA Centaur CP, Siemens |
| Models | 01157807, 10491379, 10310434, 10378883, 10328931, 06489701, 10309044, 10331250, 10310308, 10340209, 64.4—78.80F, 09010686 and 42 more |
| Date | Nov 26, 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