Corflex recalls CONTENDER POST-OP-KNEE BRACE FULL FOAM Model: 75-7550-000 Post-Operative Knee Brace is indicated for range of motion c

Recalled January 13, 2016 · FDA recall Z-0580-2016 · 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

80 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

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 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 →