{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "The affected products are labeled as a 62.5mm LEFT Femur; however, the contents are a Vanguard 70mm RIGHT Femur.",
      "address_2": "",
      "product_quantity": "8",
      "code_info": "Item #183066/Lot 132900; UDI-(01) 0088030427068 (17) 270816 (10) 132900",
      "center_classification_date": "20180314",
      "distribution_pattern": "US Distribution to states of: FL, WI, MD, MO, and MI.",
      "state": "IN",
      "product_description": "Vanguard CR Porous Femoral 62.5mm (Left Femur)     For use in total knee arthroplasty",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-1011-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79250",
      "termination_date": "20180823",
      "more_code_info": "",
      "recall_initiation_date": "20171003",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}