{
  "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": "Warsaw",
      "state": "IN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "71549",
      "recalling_firm": "Biomet, Inc.",
      "address_1": "56 E Bell Dr",
      "address_2": "N/A",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic: TX NJ, NC, KY, MA, SD, MO, AL, IN, GA, AR  International: Netherlands, Japan, Costa Rica",
      "recall_number": "Z-2072-2015",
      "product_description": "A.L.P.S. - Medium Bone Plate Forceps.  Orthopedic manual surgical instrument.",
      "product_quantity": "223",
      "reason_for_recall": "Medium Bone Plate Forceps was assembled with the incorrect grip arm tip.  Potential that the surgeon will be unable to provisionally clamp the plate to the patient's bone.",
      "recall_initiation_date": "20150617",
      "center_classification_date": "20150714",
      "termination_date": "20160322",
      "report_date": "20150722",
      "code_info": "Part Number: 816301006  Lot Numbers: 099216, 093776, 093717, 093716, 088526, 081179, 072525, 072524",
      "more_code_info": ""
    }
  ]
}