International safety notice
Urgent field safety notice for RAPIDPoint 400 / 405 / 500 and RAPIDLab 1200 systems, Siemens Healthcare Diagnostics Inc.
Germany / BfArM · DEU · Sep 14, 2016
Key facts
| Title | Urgent field safety notice for RAPIDPoint 400 / 405 / 500 and RAPIDLab 1200 systems, Siemens Healthcare Diagnostics Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | RAPIDPoint 400 / 405 / 500 and RAPIDLab 1200 systems, Siemens Healthcare Diagnostics Inc. |
| Manufacturer | Urgent field safety notice for RAPIDPoint 400 / 405 / 500 and RAPIDLab 1200 systems, Siemens Healthcare Diagnostics Inc. |
| Models | 10696857, 10339634, 10470366, DQSP-00003-T1V2.0, 10492730, 10321844, 10321852, 10337179, 10321238, 16-021.A.US.-OUS, 02062, 10310464 and 28 more |
| Date | Sep 14, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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