International safety notice

Correction Notice for VITEK® 2 Antimicrobial Susceptibility Test Kits (AST), bioMérieux, Inc.

Germany / BfArM · DEU · May 4, 2015

Key facts

Title Correction Notice for VITEK® 2 Antimicrobial Susceptibility Test Kits (AST), bioMérieux, Inc.
Regulator Germany / BfArM
Country DEU
Brand VITEK® 2 Antimicrobial Susceptibility Test Kits (AST), bioMérieux, Inc.
Manufacturer Correction Notice for VITEK® 2 Antimicrobial Susceptibility Test Kits (AST), bioMérieux, Inc.
Models AST-YS06, 6258™, 414967, 22108, 412610, FCT02N, AST-YS07, FCT01N, AST-YS01
Date May 4, 2015
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models in FDA data
  • 10–99 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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