International safety notice

Ensayo Aptima Combo 2 (AC2) utilizado en los sistemas Tigris® DTS® y Panther®, números de catálogo 301130, 302923 y 303094.

Spain / AEMPS · ESP · Jun 25, 2019

Key facts

Title Ensayo Aptima Combo 2 (AC2) utilizado en los sistemas Tigris® DTS® y Panther®, números de catálogo 301130, 302923 y 303094.
Regulator Spain / AEMPS
Country ESP
Brand Ensayo Aptima Combo 2 (AC2) utilizado en los sistemas Tigris® DTS® y Panther®, números de catálogo 301130, 302923 y 303094.
Manufacturer Hologic Inc, EEUU.
Models 303091, X1000, COMBO2, RLU≥15, 28022, 303094, 2019-337, 52862, APTIMACOMBO2, 301130, 28050, FA-00095 and 5 more
Event type Safety Notice
Date Jun 25, 2019

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