{
  "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": "71850",
      "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 Canada and Japan.",
      "recall_number": "Z-2483-2015",
      "product_description": "Vision RingLoc Shell 50 mm Size 23.   Hip joint replacement prosthesis.",
      "product_quantity": "5",
      "reason_for_recall": "The device was assembled without screw hole plugs.",
      "recall_initiation_date": "20150728",
      "center_classification_date": "20150829",
      "termination_date": "20160517",
      "report_date": "20150909",
      "code_info": "Part Number:135250; Lot Number:946410"
    }
  ]
}