International safety notice
Sistemas de monitorización de paciente Philips Xper Flex Cardio, modelos FC2010 y FC2020.
Spain / AEMPS · ESP · Jan 31, 2019
Key facts
| Title | Sistemas de monitorización de paciente Philips Xper Flex Cardio, modelos FC2010 y FC2020. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de monitorización de paciente Philips Xper Flex Cardio, modelos FC2010 y FC2020. |
| Manufacturer | Philips Medical Systems, Estados Unidos. |
| Models | 2019-056, 28022, Y453564669081, REFERENCIA453564241901, 453564669081, 5.416, FC2020, FSN86400025A_FCO72200435, 453564621801, A-28017143, 453564241911, 49971 and 9 more |
| Event type | Safety Notice |
| Date | Jan 31, 2019 |
At a glance
- No Recall
- Yes Field safety notice
- 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