International safety notice

Tarjetas de identificación (ID)/ Prueba de Sensibilidad Antimicrobiana (AST) VITEK® 2

Spain / AEMPS · ESP · Feb 7, 2019

Key facts

Title Tarjetas de identificación (ID)/ Prueba de Sensibilidad Antimicrobiana (AST) VITEK® 2
Regulator Spain / AEMPS
Country ESP
Brand Tarjetas de identificación (ID)/ Prueba de Sensibilidad Antimicrobiana (AST) VITEK® 2
Manufacturer bioMérieux Inc., EEUU.
Models 2440811203, 2880809203, 25-FEB-20, 21347, 50166, 24-AUG-18, 16-AUG-18, 420739, 21341, 91.822.52.89, 45-47, 22-FEB-20 and 29 more
Event type Safety Notice
Date Feb 7, 2019

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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