International safety notice
Sistemas de Ultrasonido Philips EPIQ, modelos EPIQ Elite EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx y EPIQ CVxi, enviados entre el 16/01/2019 y el 22/10/2020
Spain / AEMPS · ESP · Feb 10, 2021
Key facts
| Title | Sistemas de Ultrasonido Philips EPIQ , modelos EPIQ Elite EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx y EPIQ CVxi, enviados entre el 16/01/2019 y el 22/10/2020 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de Ultrasonido Philips EPIQ , modelos EPIQ Elite EPIQ 5G, EPIQ 5C, EPIQ 5W, EPIQ 7G, EPIQ 7C, EPIQ 7W, EPIQ CVx y EPIQ CVxi, enviados entre el 16/01/2019 y el 22/10/2020 |
| Manufacturer | Philips Ultrasound Inc., Estado Unidos |
| Models | 2021-072, 65545, 28050, 28022, FCO79500546, 91.822.52.89, A-28017143, “FCO79500546, FSN79500546, 12082, 5.416 |
| Event type | Safety Notice |
| Date | Feb 10, 2021 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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