International safety notice

Desfibrilador Externo Automático Philips HS1 Onsite

Spain / AEMPS · ESP · Mar 9, 2021

Key facts

Title Desfibrilador Externo Automático Philips HS1 Onsite
Regulator Spain / AEMPS
Country ESP
Brand Desfibrilador Externo Automático Philips HS1 Onsite
Manufacturer Philips Medical Systems, EEUU.
Models A-28017143, 91.822.52.89, 28022, 66576, “FCO86100229, 28050, 5.416, FSN86100229A, FCO86100229, 2021-129
Event type Safety Notice
Date Mar 9, 2021

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

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