International safety notice
Safety Notice for the Philips Allura Xper FD, Philips Healthcare
Germany / BfArM · DEU · Oct 14, 2015
Key facts
| Title | Safety Notice for the Philips Allura Xper FD, Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Philips Allura Xper FD, Philips Healthcare |
| Manufacturer | Safety Notice for the Philips Allura Xper FD, Philips Healthcare |
| Models | 722026, 722033, 722038, 722039, XCR603-150425, 2007-12-18, UXW-060003A2, 722059, 722058, 722034, 722028, 722035 and 11 more |
| Date | Oct 14, 2015 |
| 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