International safety notice

Dispositivo de fijación de malla de hernias LiquiBand FIX8 (código de producto: FX002)

Spain / AEMPS · ESP · Feb 23, 2022

Key facts

Title Dispositivo de fijación de malla de hernias LiquiBand FIX8 (código de producto: FX002)
Regulator Spain / AEMPS
Country ESP
Brand Dispositivo de fijación de malla de hernias LiquiBand FIX8 (código de producto: FX002)
Manufacturer Advanced Medical Solutions Ltd. Reino Unido
Models FX002, 77070, P00221313, P00226740, P00221600, 01606, 28043, P00221182, P00225801, P00225605, 2022-093, 545617 and 8 more
Event type Safety Notice
Date Feb 23, 2022

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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