International safety notice

Reha

United Kingdom / MHRA · GBR · Jul 10, 2017

Key facts

Title Reha
Regulator United Kingdom / MHRA
Country GBR
Brand G-EO System
Manufacturer Reha
Models 10535, 3156086, 195970, 3156094, 3156085, 92400, 3156084, 1200101, 3156076, MOD1238, 3156075, 195972 and 3 more
Event type Safety Notice
Action type Field safety notice
Date Jul 10, 2017
Regulator page gov.uk

At a glance

  • No Recall
  • Yes Field safety notice
  • 10–99 Matching device models in FDA data
  • 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

Browse all International device safety notices