International safety notice
Philips Medical
United Kingdom / MHRA · GBR · Nov 16, 2015
Key facts
| Title | Philips Medical |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Allura Xper FD R8.2.1.1 |
| Manufacturer | Philips Medical |
| Models | 722059, 722036, 722034, 722033, 722027, 722039, 722058, 722026, 722035, 722038, 722029, 722028 |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Nov 16, 2015 |
| 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