{
  "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": "2026-04-29",
    "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": "71423",
      "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: None.    International:  Netherlands and Japan",
      "recall_number": "Z-2058-2015",
      "product_description": "A.L.P.S., 3.5mm x 60 mm Cortical Locking Screw. Bone fixation screw",
      "product_quantity": "50 units",
      "reason_for_recall": "Sterile packaging was not sealed.  The implantation of an unsterile screw may lead to infection.",
      "recall_initiation_date": "20150604",
      "center_classification_date": "20150710",
      "termination_date": "20160322",
      "report_date": "20150722",
      "code_info": "Part number:856135060  Lot: 061300",
      "more_code_info": ""
    }
  ]
}