International safety notice

Sistemas Sensis, Sensis Vibe Combo y Sensis Vibe Hemo, modelos 10764561, 11007642, 11007641

Spain / AEMPS · ESP · Apr 13, 2021

Key facts

Title Sistemas Sensis, Sensis Vibe Combo y Sensis Vibe Hemo, modelos 10764561, 11007642, 11007641
Regulator Spain / AEMPS
Country ESP
Brand Sistemas Sensis, Sensis Vibe Combo y Sensis Vibe Hemo, modelos 10764561, 11007642, 11007641
Manufacturer Siemens Healthcare GmbH, Alemania
Models 28906, SOFTWAREVD12A, V17.04, 28022, 10764561, 11007641, 2021-194, AX073, 91.822.52.89, 11007642, AX074, VD12A and 1 more
Event type Safety Notice
Date Apr 13, 2021

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