{
  "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": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "The implant only has one bolt in the sterile package but it should have had two.",
      "address_2": "",
      "product_quantity": "16",
      "code_info": "Lot 320390, UDI (01) 0088030448157 (17) 230129 (10) 320390",
      "center_classification_date": "20180925",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) to the following US states:  AZ, KS, NM, NV, and UT; and to countries of:  Australia and Netherlands.",
      "state": "IN",
      "product_description": "Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment,  Model Number 185221     Intended for use in Total Knee Arthroplasty",
      "report_date": "20181003",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-3249-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80904",
      "termination_date": "20190425",
      "more_code_info": "",
      "recall_initiation_date": "20180802",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}