International safety notice

Urgent Field Safety Notice for Functional Fibrinogen Kit by Haemonetics Corporation US

Germany / BfArM · DEU · Nov 17, 2022

Key facts

Title Urgent Field Safety Notice for Functional Fibrinogen Kit by Haemonetics Corporation US
Regulator Germany / BfArM
Country DEU
Brand Functional Fibrinogen Kit
Manufacturer Haemonetics Corporation US
Models 118474-MULTI, 576.4, 02110, EP28-A3, 07-034, 444.9, FSCA-FY23-02, 113146-IE, 210.6, RCL-100341-IE
Date Nov 17, 2022
Regulator page bfarm.de

At a glance

  • No Recall
  • No 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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