International safety notice

Philips Healthcare

United Kingdom / MHRA · GBR · Apr 15, 2015

Key facts

Title Philips Healthcare
Regulator United Kingdom / MHRA
Country GBR
Brand DuraDiagnost 3.0/4.0
Manufacturer Philips Healthcare
Models 712211, 712214
Event type Safety Notice
Action type Field safety notice
Date Apr 15, 2015
Regulator page gov.uk

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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