International safety notice

Corrective action for Olympus PK7200 Blood Grouping Systems, Beckman Coulter

Germany / BfArM · DEU · Apr 6, 2010

Key facts

Title Corrective action for Olympus PK7200 Blood Grouping Systems, Beckman Coulter
Regulator Germany / BfArM
Country DEU
Brand Olympus PK7200 Blood Grouping Systems, Beckman Coulter
Manufacturer Corrective action for Olympus PK7200 Blood Grouping Systems, Beckman Coulter
Models 22-FEB-2010, 102-10-BCB, P.9-28, P.8-60, PK7200, FSW01, 02-10-BCB
Date Apr 6, 2010
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice

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