{
  "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": "567 units",
      "code_info": "Lot Number  486100  262400  291180  584260  663550  562250  666830  660450  841520  917700  966720  966720R  075450  075460  075500  663530  995960  322020  043860  090190  206820  075440  745670  352820  383680  075470  745650  513340  159230  258060  429230  161960  161950  161930  161910  161920  162010  161860  274480  161870  161900  274460  996070  274490  274510  721690  322000  456750  456750R  274470  374780  951150  075510  469490  721670  309710  274500  309680  309690  075490  309700  585540  883560  221140  374030  920540  279010  450330  672510  575980  821280  943360  599120  600770  712550  717160  017970  076400  076410  220040  175290  175290R  289160  676270  676300  228610  351290  395400  395420  445370  395400R",
      "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 67mm  Item # 195271",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2506-2019",
      "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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}