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 · Oct 30, 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.
Event type Safety Notice
Date Oct 30, 2024

At a glance

  • No Recall
  • Yes Field safety notice

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

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