{
  "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,
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  },
  "results": [
    {
      "country": "United States",
      "city": "Warsaw",
      "address_1": "56 E Bell Dr",
      "reason_for_recall": "The locking bar not fully engaging",
      "address_2": "",
      "product_quantity": "84 units",
      "code_info": "Lot Number  590540  590530  590520  663190  590550  663200  907710  117740  332690  833210  752580  373050  373060  515050  752120  515070  752100  752110  754490  764390  861210  837790  936210  764400  846520  928890  907690  936220  936230  954050  928880  936200  954030  907700  063000  062990  570980  584230",
      "center_classification_date": "20190912",
      "distribution_pattern": "State  NY  IN  OH  MI  GA  SC  FL  MO  WI  MN  ND  SD  NE  NJ  PA  MD  IL  IA  CA  VA  NC  DC  WV  AR  AL  MS  AL   MI   WA  OR  ID  LA  FL   KS  TN  MA  KY  OK  TX  TX   CT  AZ  NV  NM  MT  WY  CO  UT  DC  WY    Country:  KOREA  CHINA  CANADA  AUSTRALIA  JAPAN  EMEA  SWEDEN  ITALY",
      "state": "IN",
      "product_description": "Vanguard XP Tibial Tray 73 mm  Item # 195250",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2533-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83594",
      "termination_date": "20210416",
      "more_code_info": "",
      "recall_initiation_date": "20190815",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}