International safety notice

Recall of Coulter LH 500 Series Analyzer, Coulter HmX Hematology Analyzer, Coulter HmX Hematology Analyzer with Autoloader, Coulter MAXM Hematology Analyzer and Coulter MAXM Hematology Analyzer with Autoloader, Beckman Coulter

Germany / BfArM · DEU · Jan 19, 2012

Key facts

Title Recall of Coulter LH 500 Series Analyzer, Coulter HmX Hematology Analyzer, Coulter HmX Hematology Analyzer with Autoloader, Coulter MAXM Hematology Analyzer and Coulter MAXM Hematology Analyzer with Autoloader, Beckman Coulter
Regulator Germany / BfArM
Country DEU
Brand Recall of Coulter LH 500 Series Analyzer, Coulter HmX Hematology Analyzer, Coulter HmX Hematology Analyzer with Autoloader, Coulter MAXM Hematology Analyzer and Coulter MAXM Hematology Analyzer with Autoloader, Beckman Coulter
Manufacturer Recall of Coulter LH 500 Series Analyzer, Coulter HmX Hematology Analyzer, Coulter HmX Hematology Analyzer with Autoloader, Coulter MAXM Hematology Analyzer and Coulter MAXM Hematology Analyzer with Autoloader, Beckman Coulter
Models 526-6932, 6605527, 6605526, 6605524, 178832, LH500, 526-7694, 6705999, 6705998, 178834, 6605523, 6706000 and 14 more
Date Jan 19, 2012
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