International safety notice

Urgent Field Safety Notice for FiberTak® DX Suture Anchor, Double-Loaded With 0.9 by Arthrex INC

Germany / BfArM · DEU · Jan 12, 2024

Key facts

Title Urgent Field Safety Notice for FiberTak® DX Suture Anchor, Double-Loaded With 0.9 by Arthrex INC
Regulator Germany / BfArM
Country DEU
Brand FiberTak® DX Suture Anchor, Double-Loaded With 0.9
Manufacturer Arthrex INC
Models 15147890, 15147931, 00888867301078, AR-8990ST-1, 85235, 685235, 909005-4131, 00888867377370, AR-8990ST-2
Date Jan 12, 2024
Regulator page bfarm.de

At a glance

  • No Recall
  • No Field safety notice
  • 1–9 Matching device models 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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