International safety notice

SYNCHRON LXi 725 Clinical System

Swiss / SwissMedic · CHE · Aug 4, 2008

Key facts

Title SYNCHRON LXi 725 Clinical System
Regulator Swiss / SwissMedic
Country CHE
Brand SYNCHRON LXi 725 Clinical System
Manufacturer Beckman Coulter, Inc.
Models 2125A, 0825-33-39-39, ormat1.on, 333-5, 333.5, 1111111111111111111111111111111, Verschleil5, D-47807, 601469, 20000, 81910, Verschleif1 and 37 more
Event type Safety Notice
Date Aug 4, 2008
Regulator page fsca.swissmedic.ch

At a glance

  • No Recall
  • Yes Field safety notice
  • 100–999 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

Browse all International device safety notices