Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0574-2016 — Corflex Contender Post-Op Knee Brace Lite Model: 75-7500-000 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 repl

U.S. FDA — Device Enforcement · United States · 2015-11-12 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0574-2016
Date of alert: 2015-11-12
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Corflex
Product category: device
Product type: Devices

Reported risk: 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,

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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