International safety notice
Philips
United Kingdom / MHRA · GBR · Dec 1, 2018
Key facts
| Title | Philips |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Intera, Enterprise, Achieva, Achieva XT, Achieva Conversion, Panorama HFO, Ingenia, Smartpath to dStream, Multiva, Prodiva, MR-OR, MR-RT, MR-Linac and MR-Marlin MR systems. |
| Manufacturer | Philips |
| Models | 781474, 453564621801, 781104, 781174, 781069, 781262, 781346, 781343, 781357, 781359, 781160, 781070 and 61 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Dec 1, 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