International safety notice
Corrective action for the Philips MobileDiagnost wDR X-ray systems, Philips Medical Systems
Germany / BfArM · DEU · Jun 25, 2014
Key facts
| Title | Corrective action for the Philips MobileDiagnost wDR X-ray systems, Philips Medical Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Philips MobileDiagnost wDR X-ray systems, Philips Medical Systems |
| Manufacturer | Corrective action for the Philips MobileDiagnost wDR X-ray systems, Philips Medical Systems |
| Models | 71200110, XI-DXR-200-5004, 2014-APRIL-08, FCO-71200110 |
| Date | Jun 25, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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