HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038… — Class II medical device recall Z-0576-2016
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-0576-2016 |
|---|---|
| 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 | 4 units |
| Model numbers | 75-7500-038 |
Product
HAILEY ORTHO CONTENDER POST-OP-KNEE BRACE Model : 75-7500-038 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-0576-2016. 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.