International safety notice
Corrective action for the Allura Xper Systems (Monitor Ceiling Suspension), Philips Healthcare
Germany / BfArM · DEU · Aug 19, 2015
Key facts
| Title | Corrective action for the Allura Xper Systems (Monitor Ceiling Suspension), Philips Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Allura Xper Systems (Monitor Ceiling Suspension), Philips Healthcare |
| Manufacturer | Corrective action for the Allura Xper Systems (Monitor Ceiling Suspension), Philips Healthcare |
| Models | 72201, 722013, 722024, THC8AWDS-122, FC072200279, XCR603-150381, 722023, 989600-184-665, 722010, 989600-184-654, THC8AWDS-121, XCR603-1 and 4 more |
| Date | Aug 19, 2015 |
| 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