{
  "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": "Vanguard Knee System Series-A Standard Patella a potential commingle that could result in the size of the implant not matching the size on the label.",
      "address_2": "",
      "product_quantity": "45 units",
      "code_info": "Lot Number: 399960  UDI Number: (01)00880304431317(17)230302(10)399960",
      "center_classification_date": "20190223",
      "distribution_pattern": "MN, VA  Foreign: Korea, New Zealand and Japan",
      "state": "IN",
      "product_description": "Vanguard Knee System Series-A Standard Patella sizes 31mm  Item Number: 184764",
      "report_date": "20190306",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-0937-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "82004",
      "termination_date": "20200513",
      "more_code_info": "",
      "recall_initiation_date": "20181221",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}