International safety notice

Urgent Field Safety Notice for Phadia 200, Fluorescent immunoassay analyser IVD, laboratory by Phadia AB

Germany / BfArM · DEU · May 9, 2022

Key facts

Title Urgent Field Safety Notice for Phadia 200, Fluorescent immunoassay analyser IVD, laboratory by Phadia AB
Regulator Germany / BfArM
Country DEU
Brand Phadia 200, Fluorescent immunoassay analyser IVD, laboratory
Manufacturer Phadia AB
Models RNP70, 75137, 758393, QA2022-02, LKM-1, 07333066016900, 12-4300-00, U1RNP, FSN2022-02, SCL-70S, 7-230, 758187
Date May 9, 2022
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

Browse all International device safety notices