International safety notice
Philips Healthcare
United Kingdom / MHRA · GBR · Mar 13, 2018
Key facts
| Title | Philips Healthcare |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Allura Xper / UNIQ |
| Manufacturer | Philips Healthcare |
| Models | 722029, 722025, 722039, 722035, 722033, 722012, 722022, 722026, 722024, 722023, 722058, 722008 and 15 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Mar 13, 2018 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes 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