{
  "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": "2026-04-01",
    "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": "88304",
      "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": "US Nationwide distribution.",
      "recall_number": "Z-2269-2021",
      "product_description": "Arcos Modular Revision Hip System Standard Cone Prox Body, Size E, 70 MM\t    Item Number:11-301325",
      "product_quantity": "11 units",
      "reason_for_recall": "Arcos Proximal Cone Bodies could potentially exhibit chatter in the inner taper fretting corrosion  and device failure in vivo leading to surgical intervention",
      "recall_initiation_date": "20210602",
      "center_classification_date": "20210812",
      "termination_date": "20220706",
      "report_date": "20210818",
      "code_info": "Lot Numbers/UDI : 880850 (01)00880304480575(17)310412(10)880850"
    }
  ]
}