{
  "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": "2026-04-08",
    "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": "81472",
      "recalling_firm": "Zimmer 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": "AR, MO, MN, NJ, NY, OH,   MN , NJ,  VA",
      "recall_number": "Z-0496-2019",
      "product_description": "Vanguard Knee System -PS Open Box Femoral   Right, 65 mm  Item Number:183108",
      "product_quantity": "8 units",
      "reason_for_recall": "Label on the outer carton or the patient labels does not match label on the inner sterile packaging",
      "recall_initiation_date": "20181022",
      "center_classification_date": "20181121",
      "termination_date": "20191211",
      "report_date": "20181128",
      "code_info": "Lot Number: J6265594  UDI: (01)00880304270893(17)280411(10)J6255863",
      "more_code_info": ""
    }
  ]
}