International safety notice

Paquetes de reactivos auxiliares utilizados en los analizadores: Atellica IM 1300, referencia 11066001 y Atellica IM 1600, referencia 11066000

Spain / AEMPS · ESP · Oct 8, 2021

Key facts

Title Paquetes de reactivos auxiliares utilizados en los analizadores: Atellica IM 1300, referencia 11066001 y Atellica IM 1600, referencia 11066000
Regulator Spain / AEMPS
Country ESP
Brand Paquetes de reactivos auxiliares utilizados en los analizadores: Atellica IM 1300, referencia 11066001 y Atellica IM 1600, referencia 11066000
Manufacturer Siemens Healthcare Diagnostics Inc, EEUU.
Models 72910, 11066001ATELLICA, 21-07.A.OUS, 2021-552, 02032, 11066001, 11208742, 11066000, 91.822.52.89, 28906, 28022
Event type Safety Notice
Date Oct 8, 2021

At a glance

  • No Recall
  • Yes 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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