{
  "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": {
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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": "480 units",
      "code_info": "Lot Number  522520  571140  589700  758150  028960  028980  043970  028980R  043970R  064960  028970  065200  101860  101880  065200R  433940  321620  321640  321620R  321640R  433910  592120  592140  592150  592170  257970  592180  801960  282710  282710R  282690  801940  801950  783060  783040  011410  975550  592110  984660  023340  257960  840190  061310  592160  102990  223050  261130  336080  585400  585370  511430  467140  684820  664140  634080  705510  715730  716030  716030R  920550  881940  029210  906640  985880  072790  125870  162880  396240  318430  247250  336660  441870  374320  587220  509590  543180  543150  708390  576080  639600  670510  522580  558990  593560  450400  741460  758480  780160  808130  833150  873470  943480  850880  917590  183370  560280  570170  570180  570180R  076640  191080  111620  950910  963430  999270  018060  261910  613310  650370",
      "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-XP Tibial Tray - Interlok 63 mm  Item # 195751",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2526-2019",
      "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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}