{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "1800 W Center St",
      "reason_for_recall": "During a transfer of products from a recently shutdown facility, the firm discovered raw material labeled as latex free actually contained latex.",
      "address_2": "",
      "product_quantity": "131 units",
      "code_info": "Model #: 00-1746-001-00 through 00-1746-006-00",
      "center_classification_date": "20140509",
      "distribution_pattern": "Worldwide Distribution - US Nationwide in the states of: AK, AZ, CA, FL, GA, IA, IL, IN, LA, MD, MI, MO NC, NE, NV, NY, OH, OK, OR, PA, RI, SD, TX, UT, VA, VT, WA, WI & WV and countries of: AUSTRALIA, CANADA, GERMANY, IRAQ, ITALY, SAUDI ARABIA, TUNISIA & UNITES ARAB EMIRATES.",
      "state": "IN",
      "product_description": "DROP LOK\" Knee Brace***LATEX FREE\"     Product Usage:  Used in the treatment, support, and rehabilitation of many types of knee injuries or following surgical correction.",
      "report_date": "20140521",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer, Inc.",
      "recall_number": "Z-1603-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "68017",
      "termination_date": "20150414",
      "more_code_info": "",
      "recall_initiation_date": "20140319",
      "postal_code": "46580-2304",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}