International safety notice

Urgent Safety Notice for Hitachi MRI Systems AIRIS Vento, AIRIS Vento LT, APERTO Eterna, APERTO Lucent, Echelon and Oasis, Hitachi Medical Corporation

Germany / BfArM · DEU · Sep 2, 2015

Key facts

Title Urgent Safety Notice for Hitachi MRI Systems AIRIS Vento, AIRIS Vento LT, APERTO Eterna, APERTO Lucent, Echelon and Oasis, Hitachi Medical Corporation
Regulator Germany / BfArM
Country DEU
Brand Hitachi MRI Systems AIRIS Vento, AIRIS Vento LT, APERTO Eterna, APERTO Lucent, Echelon and Oasis, Hitachi Medical Corporation
Manufacturer Urgent Safety Notice for Hitachi MRI Systems AIRIS Vento, AIRIS Vento LT, APERTO Eterna, APERTO Lucent, Echelon and Oasis, Hitachi Medical Corporation
Models QAM15-013, QAM15-012, PACK7, QAM15-014, PACK8, V2.2A, V2.1ASERVICE, QAM15-015, PACK4, REV.1.5, QAM15-016, QAM15-017 and 3 more
Date Sep 2, 2015
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

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