International safety notice
Urgent field corrective action for ADVIA Centaur / ADVIA Centaur XP, Siemens Healthcare Diagnostics Inc.
Germany / BfArM · DEU · Jan 28, 2016
Key facts
| Title | Urgent field corrective action for ADVIA Centaur / ADVIA Centaur XP, Siemens Healthcare Diagnostics Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | ADVIA Centaur / ADVIA Centaur XP, Siemens Healthcare Diagnostics Inc. |
| Manufacturer | Urgent field corrective action for ADVIA Centaur / ADVIA Centaur XP, Siemens Healthcare Diagnostics Inc. |
| Models | 10329339, 10336292, 10361012, 10322731, 10361011, 10325015, 10309525, 10327638, 10316248, 10320757, 10321568, 10364455 and 50 more |
| Date | Jan 28, 2016 |
| 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