Corflex recalls

Corflex appears in 7 official U.S. recall notices indexed by RecallRadar, most recently on 2016-01-13.

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

• ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075 Post-Operative Knee Brace is indicated for range of motion control at t…
  FDA Device · Class II · 2016-01-13 · Corflex
• ADV ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-231 Post-Operative Knee Brace is indicated for range of motion control at the kn…
  FDA Device · Class II · 2016-01-13 · Corflex
• Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 Post-Operative Knee Brace is indicated for range of motion control at the knee…
  FDA Device · Class II · 2016-01-13 · Corflex
• HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 Post-Operative Knee Brace is indicated for range of motion control at the kne…
  FDA Device · Class II · 2016-01-13 · Corflex
• BRIELLE ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-087 Post-Operative Knee Brace is indicated for range of motion control at th…
  FDA Device · Class II · 2016-01-13 · Corflex
• CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011 Post-Operative Knee Brace is indicated for range of motion control at the kne…
  FDA Device · Class II · 2016-01-13 · Corflex
• CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Knee Brace is indicated for range of motion control at the knee jo…
  FDA Device · Class II · 2016-01-13 · Corflex