International safety notice
Corrective action for the Advia Centaur Systems T4 assay for Advia Centaur, Advia Centaur XP and Advia Centaur CP, Siemens
Germany / BfArM · DEU · Oct 25, 2011
Key facts
| Title | Corrective action for the Advia Centaur Systems T4 assay 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 the Advia Centaur Systems T4 assay for Advia Centaur, Advia Centaur XP and Advia Centaur CP, Siemens |
| Models | 73945147, 09236439, 78085148, 73514147, XXXXXX146, 74576147, 71336146, 73072146, 10591, 71392146, 71844146, XXXXX146 and 16 more |
| Date | Oct 25, 2011 |
| 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