{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "85205",
      "recalling_firm": "Philips North  America, LLC",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution: US (nationwide) including the following states: Arkansas, Arizona, California, Colorado, Delaware, Florida, Georgia, Illinois, Indiana, Kentucky, Massachusetts, Maryland, Michigan, Minnesota, Missouri, Mississippi, North Carolina, Nebraska, New Jersey, Nevada, New York, Ohio, Oregon, Pennsylvania, Puerto Rico, Texas, Virginia, Wisconsin. And the following Countries of: Australia, Azerbaijan, Chile, Croatia, Czechoslovakia, Denmark, Finland, France, Germany, India, Israel,  Italy, Japan, Korea South, Lebanon, Mexico, Netherlands, Norway, Pakistan, Poland, Russian Federate, Senegal, Spain, South Africa, Sweden, Switzerland, Taiwan,  and Uruguay.",
      "recall_number": "Z-1801-2020",
      "product_description": "Phillips Azurion 7 M20, Angiographic X-Ray System Code 722079    Image guidance in diagnostic, interventional and minimally invasive surgery procedures for the following clinical application areas: vascular, non-vascular, cardiovascular and neuro procedures.",
      "product_quantity": "162 units",
      "reason_for_recall": "No torque was specified for the four screws that connect the gearbox and the mounting flange within the C-arm roll motor which could result in the screws becoming loose..",
      "recall_initiation_date": "20200305",
      "center_classification_date": "20200424",
      "termination_date": "20220909",
      "report_date": "20200506",
      "code_info": "Serial Numbers:   709,  710,  711,  713,  716,  715,  439,  526,  637,  653,  684,  621,  497,  792,  595,  674,  737,  628,  429,  605,  895,  540,  769,  668,  697,  758,  633,  520,  738,  691,  813,  428,  590,  706,  611,  655,  804,  663,  588,  877,  854,  654,  488,  836,  689,  717,  790,  629,  598,  736,  810,  841,  946,  795,  673,  776,  645,  646,  703,  608,  805,  746,  262,  730,  753,  878,  755,  837,  618,  594,  714,  543,  751,  263,  766,  817,  741,  534,  535,  536,  466    System Equipment Numbers:  74620447,  74620437,  74613625,  74613538,  74620341,  77839007,  73340583,  73326701,  77646555,  77559977,  77970948,  77427180,  72722066,  79132604,  72273457,  76100048,  77970800,  74620302,  72805859,  77228623,  80018072,  74611961,  77647014,  75486269,  78248928,  75486357,  76888124,  75581571,  78243622,  75423992,  77971015,  74817549,  76890243,  74352012,  77260210,  77213972,  78993356,  77347585,  75532686,  79152378,  79109118,  75533239,  74536213,  79152254,  77838972,  78150020,  78696158,  77559984,  76481840,  75848181,  79112403,  77905831,  80171865,  79042710,  77697096,  77213970,  74778339,  74778897,  73051857,  73717291,  78132484,  75305793,  72312081,  76890941,  76888973,  78365267,  76888978,  79464469,  72323525,  72323935,  74169336,  74620425,  76891009,  72417922,  79035318,  79035262,  78367631,  74584486,  74584491,  75615010,  75470091"
    }
  ]
}