International safety notice

Analizador de inmunoensayos Phadia 1000, número de artículo 12-3800-01

Spain / AEMPS · ESP · Jul 23, 2019

Key facts

Title Analizador de inmunoensayos Phadia 1000, número de artículo 12-3800-01
Regulator Spain / AEMPS
Country ESP
Brand Analizador de inmunoensayos Phadia 1000, número de artículo 12-3800-01
Manufacturer Phadia AB, Suecia.
Models 609425060, FSN2019-04, 28022, 08174, 7-102, 935896968, 1.200, 91.822.52.89, 2019-379, 53436, 12-3800-01
Event type Safety Notice
Date Jul 23, 2019

At a glance

  • No Recall
  • Yes 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

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