International safety notice

• Sistemas de inmunoanálisis UniCel Dxl 600 (Referencias A30260, A71460, A71461, A92060) • Sistemas de inmunoanálisis UniCel Dxl 800 (Referencias 973100, A71456, A71457, A84545, A25288, A25285) • Sistemas clínicos UniCel DxC 660i, 680i, 860i y 880i Access

Spain / AEMPS · ESP · Jan 24, 2019

Key facts

Title • Sistemas de inmunoanálisis UniCel Dxl 600 (Referencias A30260, A71460, A71461, A92060) • Sistemas de inmunoanálisis UniCel Dxl 800 (Referencias 973100, A71456, A71457, A84545, A25288, A25285) • Sistemas clínicos UniCel DxC 660i, 680i, 860i y 880i Access
Regulator Spain / AEMPS
Country ESP
Brand • Sistemas de inmunoanálisis UniCel Dxl 600 (Referencias A30260, A71460, A71461, A92060) • Sistemas de inmunoanálisis UniCel Dxl 800 (Referencias 973100, A71456, A71457, A84545, A25288, A25285) • Sistemas clínicos UniCel DxC 660i, 680i, 860i y 880i Access
Manufacturer Beckman Coulter Inc., Estados Unidos.
Models 973100, A71457, A92060, A25285, “5.1”, A25288, 5.3.0, A64935, 41-43, A59102, 08908, A64871 and 14 more
Event type Safety Notice
Date Jan 24, 2019

At a glance

  • No Recall
  • Yes 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