{
  "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": "Draper",
      "address_1": "12187 Business Park Dr",
      "reason_for_recall": "A femoral component containing pegs was found in a box for the pegless version.",
      "address_2": "",
      "product_quantity": "5",
      "code_info": "Lot No. A131876",
      "center_classification_date": "20140512",
      "distribution_pattern": "US Nationwide Distribution in the states of NV, and AZ.",
      "state": "UT",
      "product_description": "PS-C Femoral Nonporous Rt Sz 6, Model  Number 161-1604 Component of the Balanced Knee System and Balanced Knee Revision System, for total knee arthroplasty procedures.",
      "report_date": "20140521",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Ortho Development Corporation",
      "recall_number": "Z-1610-2014",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "68029",
      "termination_date": "20140714",
      "more_code_info": "",
      "recall_initiation_date": "20140401",
      "postal_code": "84020-8663",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}