{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Andover",
      "address_1": "3000 Minuteman Road",
      "reason_for_recall": "An inspection of IATD (Installation Acceptance Test Document)IA SID (Source Image Distance) records shows table height measurements out of specification with the consequence of potential system mis-alignment",
      "address_2": "",
      "product_quantity": "116 units",
      "code_info": "Serial Numbers:  334584  345869  349805  352617  375957/SN07000650  352645  355617  356954  363678  362217  362252  361021  364214  362429  361526  363545  363802  364816  366510  366090  367504  370290  370643  373506  372845  376998  383090  384688/SN07000603  386397/SN07000659  406161/SN08000556  386265/SN08000415  389969/SN08000090  381103/SN08000131  444254/SN09000380  406491/SN08000315  389383/SN08000100  447038/SN10000169  389970/SN08000092  406017/SN08000307  389972/SN08000080  389656/SN08000052  386679/SN08000051  390255/SN08000050  394368/SN08000196  396406/SN08000193  399529/SN08000297  401268/SN08000268  402249/SN08000323  399571/SN08000559  384510/SN07000618  402246/SN08000261  403330/SN08000296  403648/SN08000292  407890/SN08000377  405887/SN08000381  413307/SN08000521  413205/SN08000562  411311/SN08000528  419318/SN09000042  428504/SN09000200  413818/SN08000526  414461/SN08000518  414601/SN08000501  438511/SN10000166  414315/SN08000474  418205/SN08000568  419316/SN09000007  421970/SN09000058  422097/SN09000068  426137/SN09000109  430918/SN09000175  435194/SN09000234  439546/SN09000334  439739/SN09000346  436337/SN09000251  438835/SN09000295  439098/SN09000294  439817/SN09000318  443072/SN09000363  443231/SN09000368  442855/SN09000357  443453/SN09000378  456506/SN10000167  449719/SN10000034  448152/SN10000013  448150/SN10000072  449717/SN10000068  450554/SN10000096  451156/SN10000059  456283/SN10000272  456082/SN10000174  458580/SN10000196  459495/SN10000212  460074/SN10000260  460485/SN10000228  460757/SN10000290  461677/SN10000302  461229/SN10000218  462389/SN10000252  463385/SN10000344  465974/SN10000320  468064/SN10000347  466164/SN10000336  468078/SN11000032  468518/SN10000353  470291/SN10000374  471046/SN10000386  471701/SN11000054  483054/SN11000246  476276/SN11000045  480210/SN11000126  483867/SN11000298  483244/SN11000199  486144/SN11000217  488176/SN11000244",
      "center_classification_date": "20130617",
      "distribution_pattern": "Worldwide Distribution - US Nationwide and the country of Canada.",
      "state": "MA",
      "product_description": "Philips BuckyDiagnost Radiographic.        Catalog Numbers:    704031, 704032, 704035, 704060, 704062      This system is used for making x-ray exposures for diagnostics",
      "report_date": "20130626",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare Inc.",
      "recall_number": "Z-1450-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "64128",
      "termination_date": "20131015",
      "more_code_info": "",
      "recall_initiation_date": "20130116",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}