{
  "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": "74025",
      "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": "Distributed in the US states of CA, GA, MN, and OH, and in the Netherlands.",
      "recall_number": "Z-1814-2016",
      "product_description": "PerFuse Decompression Instrument PN: 800-0541, Lot:100650.  Designed to access the femoral head for decompression.",
      "product_quantity": "22",
      "reason_for_recall": "The Trocar and Plunger Assemblies are missing from the instrument, which could result in a delay in surgery greater than 30 minutes.",
      "recall_initiation_date": "20160411",
      "center_classification_date": "20160525",
      "termination_date": "20170530",
      "report_date": "20160601",
      "code_info": "PerFuse Decompression Instrument PN: 800-0541, Lot:100650"
    }
  ]
}