International safety notice

Further Safety Information regarding Dade® Actin® Activated Cephaloplastin Reagent, Siemens Healthcare Diagnostics

Germany / BfArM · DEU · Aug 20, 2015

Key facts

Title Further Safety Information regarding Dade® Actin® Activated Cephaloplastin Reagent, Siemens Healthcare Diagnostics
Regulator Germany / BfArM
Country DEU
Brand Further Safety Information regarding Dade® Actin® Activated Cephaloplastin Reagent, Siemens Healthcare Diagnostics
Manufacturer Further Safety Information regarding Dade® Actin® Activated Cephaloplastin Reagent, Siemens Healthcare Diagnostics
Models 557139A, B4218-1, 557145A, 557115B, 557115A, 557136, 557115, 557142, 557137, 557139, 557116, BR-06215 and 6 more
Date Aug 20, 2015
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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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