International safety notice
Recall of Allura Xper R8.2 and UNIQ R1.0 X-ray Systems, Philips Image Guided Therapy Systems
Germany / BfArM · DEU · Jul 26, 2016
Key facts
| Title | Recall of Allura Xper R8.2 and UNIQ R1.0 X-ray Systems, Philips Image Guided Therapy Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Allura Xper R8.2 and UNIQ R1.0 X-ray Systems, Philips Image Guided Therapy Systems |
| Manufacturer | Recall of Allura Xper R8.2 and UNIQ R1.0 X-ray Systems, Philips Image Guided Therapy Systems |
| Models | 722038, 722027, PH5293857, 722026, 722034, 722028, 722039, 722059, 722035, 722058, 722033, 722029 and 1 more |
| Date | Jul 26, 2016 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 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