International safety notice
BiPAP A40 Pro, BiPAP A40 EFL, BiPAP A30 EFL. Ver números de referencia afectados en la nota de aviso de la empresa.
Spain / AEMPS · ESP · Aug 2, 2024
Key facts
| Title | BiPAP A40 Pro, BiPAP A40 EFL, BiPAP A30 EFL. Ver números de referencia afectados en la nota de aviso de la empresa. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | BiPAP A40 Pro, BiPAP A40 EFL, BiPAP A30 EFL. Ver números de referencia afectados en la nota de aviso de la empresa. |
| Manufacturer | Philips Respironics, Inc, EEUU. |
| Models | CAX3000B12, NDX3000T19, IAX3100T19, INX3100H19, REEX3000S19, CNX3000S17, DSX3000S11, 41016, DEX3100S13, RITX3100S21, KRX3000T19, KRX3000H19 and 114 more |
| Event type | Safety Notice |
| Date | Aug 2, 2024 |
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