CT ORTHO CONTENDER POST-OP-KNEE BRACE LITE Model: 75-7500-011… — Class II medical device recall Z-0575-2016

Terminated recall by Corflex, reported 2016-01-13, distributed nationwide. Knee brace could fail to maintain the locked position and a loss of balance or undesired flexion/extension may

Recall number	`Z-0575-2016`
Product type	Medical device
Classification	Class II
Status	Terminated
Voluntary or mandated	Voluntary
Recalling firm	Corflex, Manchester, NH, United States
Recall initiated	2015-11-12
Classified	2016-01-04
Reported by FDA	2016-01-13
Terminated	2016-06-29
Distributed	Nationwide (US)
Countries outside the US	CA, GB, SG, TW
Quantity	6 units
Model numbers	`75-7500-011`

Product

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 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. 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.

Reason for recall

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,

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0575-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.