FDANovember 12, 2015device

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 knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee r...

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may occur at the affected knee joint,

What to do

FDA enforcement status: Terminated

Brands named

corflex

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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