International safety notice
Interruptores de pedal inalámbricos de los sistemas Philips Allura Xper y Azurion. Ver números de modelos afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Jul 17, 2023
Key facts
| Title | Interruptores de pedal inalámbricos de los sistemas Philips Allura Xper y Azurion. Ver números de modelos afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Interruptores de pedal inalámbricos de los sistemas Philips Allura Xper y Azurion. Ver números de modelos afectados en la nota de aviso de la empresa. |
| Manufacturer | Philips Medical Systems Nederland BV, Países Bajos. |
| Models | 452300121971, 452300121811, 452220412821, 459800415534, 452220412791, 459800415532, 452300121891, 459800772261, 452220412601, 452220412731, 452220412621, 452220412561 and 79 more |
| Event type | Safety Notice |
| Date | Jul 17, 2023 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models 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