International safety notice
Philips Medical Systems
United Kingdom / MHRA · GBR · Dec 12, 2019
Key facts
| Title | Philips Medical Systems |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | Azurion system, R1.2.x and R2.0.x |
| Manufacturer | Philips Medical Systems |
| Models | 12-DECEMBER-2019, 722068, R1.2.X, 7722067, R2.0.X, 722079, 722078, 722064, 722065, 722066, 2019-IGTBST-019, 722063 and 3 more |
| Event type | Safety Notice |
| Action type | Field safety notice |
| Date | Dec 12, 2019 |
| Regulator page | gov.uk |
At a glance
- No Recall
- Yes 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