International safety notice
Corrective action for RapidPoint 400 Series, RapidPoint 500 and RapidLab 1200 Series Analyzers, Siemens
Germany / BfArM · DEU · Dec 6, 2013
Key facts
| Title | Corrective action for RapidPoint 400 Series, RapidPoint 500 and RapidLab 1200 Series Analyzers, Siemens |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | RapidPoint 400 Series, RapidPoint 500 and RapidLab 1200 Series Analyzers, Siemens |
| Manufacturer | Corrective action for RapidPoint 400 Series, RapidPoint 500 and RapidLab 1200 Series Analyzers, Siemens |
| Models | 1-877-229-3711, 10591, 30652, 914-631-8000, 631-7597, 13-73 |
| Date | Dec 6, 2013 |
| 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