International safety notice

TEG® 5000 Reactivo de Fibrinógeno Funcional, referencia 07-034.

Spain / AEMPS · ESP · May 11, 2022

Key facts

Title TEG® 5000 Reactivo de Fibrinógeno Funcional, referencia 07-034.
Regulator Spain / AEMPS
Country ESP
Brand TEG® 5000 Reactivo de Fibrinógeno Funcional, referencia 07-034.
Manufacturer Haemonetics Corporation, EEUU.
Models 2022-231, 28022, 113146, 79650, 91.822.52.89, 118474-MULTI, 1EB760A8-9850-423D-B905-713B4D7E511A, 08029, 444.9, 210.6, 576.4, 07-034 and 3 more
Event type Safety Notice
Date May 11, 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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