International safety notice
Urgent Field Safety Notice for MultiDiagnost Eleva with Flat Detector, Allura Xpe by Philips Medical Systems Nederland B.V
Germany / BfArM · DEU · Mar 18, 2019
Key facts
| Title | Urgent Field Safety Notice for MultiDiagnost Eleva with Flat Detector, Allura Xpe by Philips Medical Systems Nederland B.V |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | MultiDiagnost Eleva with Flat Detector, Allura Xpe |
| Manufacturer | Philips Medical Systems Nederland B.V |
| Models | 722020, 722008, 722026, 722039, 722003, 722011, 722058, 722010, 2017-1GTBST-029, 47INCHES, 722013, 722038 and 16 more |
| Date | Mar 18, 2019 |
| 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