Blue Belt Technologies Mn recalls

Blue Belt Technologies Mn appears in 4 official U.S. recall notices indexed by RecallRadar, most recently on 2014-07-09.

Company names are normalized from agency data (legal suffixes removed), so related firms may appear under separate pages.

• Stride Femoral Component Size 2, PFSI-00053, Right Lateral /Left Medial
  FDA Device · Class II · 2014-07-09 · Blue Belt Technologies Mn
• Stride Femoral Component Size 2, PFSI-00054, Right Medial /Left Lateral
  FDA Device · Class II · 2014-07-09 · Blue Belt Technologies Mn
• NavioPFSTM System, Orthopedic Sterotaxic Instrument, model #'s NPFS-02000, NPFS-02010, NPFS 02020
  FDA Device · Class II · 2014-05-21 · Blue Belt Technologies Mn
• Blue Belt Technologies, Inc
  FDA Device · Class II · 2013-08-28 · Blue Belt Technologies Mn