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Corflex recalls ORTHO SPEC GRP CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-075 Post-Operative Knee Brace is indicated for range o
Recalled January 13, 2016 · FDA recall Z-0577-2016 · Corflex
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, · FDA Class II
Units
42 units
Sold at
Worldwide Distribution - US (nationwide) and Internationally to Canada , Taiwan , Singapore , and England.
Description
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,
Product
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 the knee joint following ACL, PCL, MCL, and LCL surgeries, meniscal repairs, patella realignment, regenerative chondroplasty, stable femoral fractures, total knee replacements, and high tibial osteotomies.
Manufacturer(s)
Corflex
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →