{
  "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": "82 units",
      "code_info": "Lot Number  262480  960510  274400  274430  336060  336060R  274390  274410  279280  394540  394590  394570  821400  903420  960530  422490  512590",
      "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": "XP-CR Tibial Tray - Interlok 91 mm  Item # 195279",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2514-2019",
      "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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}