International safety notice

Urgent Field Safety Notice for Dornier Gemini by Dornier MedTech Systems GmbH

Germany / BfArM · DEU · Mar 14, 2018

Key facts

Title Urgent Field Safety Notice for Dornier Gemini by Dornier MedTech Systems GmbH
Regulator Germany / BfArM
Country DEU
Brand Dornier Gemini
Manufacturer Dornier MedTech Systems GmbH
Models 2018-01-08, TOIFC6183C, 888-0, 183642248, 6572-6068, 114520, D-82234, 608526, 888-107, 888-665, D-82231, 1211842 and 2 more
Date Mar 14, 2018
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 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

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