International safety notice

BV Endura versión 2.3, modelo 718075, BV Pulsera versión 2.3, modelo 718095 y Veradius Unity versión 2.1, modelo 718132

Spain / AEMPS · ESP · Jan 7, 2022

Key facts

Title BV Endura versión 2.3, modelo 718075, BV Pulsera versión 2.3, modelo 718095 y Veradius Unity versión 2.1, modelo 718132
Regulator Spain / AEMPS
Country ESP
Brand BV Endura versión 2.3, modelo 718075, BV Pulsera versión 2.3, modelo 718095 y Veradius Unity versión 2.1, modelo 718132
Manufacturer Philips Medical Systems Netherlands BV, Países Bajos
Models 2022PUEDE, 28022, 718132, 9.2.6, 718075BV, 718095VERADIUS, 28050, 3GRADO, 91.822.52.89, 718095, 2022-002, 71800092 and 7 more
Event type Safety Notice
Date Jan 7, 2022

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

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