{
  "meta": {
    "disclaimer": "Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.",
    "terms": "https://open.fda.gov/terms/",
    "license": "https://open.fda.gov/license/",
    "last_updated": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Manchester",
      "state": "NH",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "72727",
      "recalling_firm": "Corflex",
      "address_1": "669 E Ind Park Dr",
      "address_2": "N/A",
      "postal_code": "03109-5625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution - US (nationwide) and Internationally to Canada , Taiwan , Singapore , and England.",
      "recall_number": "Z-0580-2016",
      "product_description": "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.",
      "product_quantity": "80 units",
      "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,",
      "recall_initiation_date": "20151112",
      "center_classification_date": "20160104",
      "termination_date": "20160629",
      "report_date": "20160113",
      "code_info": "(1) all braces that begin with a Revision Code of AN, AP, AQ, AR, AS, AT, AU are to be returned to Corflex immediately for review; (2) all braces with a Revision Code beginning with AM and that comply with the date range:  Braces manufactured between September 1, 2015 and November 6, 2015"
    }
  ]
}