{
  "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": "384 units",
      "code_info": "Lot Number  559070  527660  677630  191210  219890  677620  758460  089950  283100  358850  283080  374620  321750  321770  358830  374580  374590  420310  420320  434060  358860  381760  321690  358840  468200  381770  381780  381780R  321710  434070  420290  468210  023420  011510  864760  093450  093460  885140  855480  975650  828760  061480  331670  103080  131270  159350  116110  223220  116110R  587400  181490  418770  634280  664240  783170  716000  906810  685020  882160  882170  881950  715990  986210  396500  986200  906820  029310  126100  163080  247440  293200  293210  163090  126090  920640  920640R  481960  073030  374570  442040  442050  318630  479060  509960  509930  450480  183670  479050  576240  543440  543450  625770  593670  639750  670660  758590  741610  481970  943600  808440  917680  951040  780300  833290  851020  873620  481950  018270  999420  076780",
      "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 83 mm  Item # 195759",
      "report_date": "20190918",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Zimmer Biomet, Inc.",
      "recall_number": "Z-2518-2019",
      "initial_firm_notification": "Letter",
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      "more_code_info": "",
      "recall_initiation_date": "20190815",
      "postal_code": "46582-6989",
      "voluntary_mandated": "Voluntary: Firm initiated",
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}