International safety notice
C-arm inspection required on certain Essenta DR X-ray systems, Philips Medical Systems
Germany / BfArM · DEU · Aug 29, 2012
Key facts
| Title | C-arm inspection required on certain Essenta DR X-ray systems, Philips Medical Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | C-arm inspection required on certain Essenta DR X-ray systems, Philips Medical Systems |
| Manufacturer | C-arm inspection required on certain Essenta DR X-ray systems, Philips Medical Systems |
| Models | XL.DXR-200-5004, SN08000092, 10000033, 2012-JU1Y-09, SN09000006, XL-DXR-200-5004, 1-800-722-9377, SN09000007, 71200068, 9890-010-87381, SN10000054, 10000014 and 1 more |
| Date | Aug 29, 2012 |
| 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