{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "27809",
      "product_res_number": "Z-0041-04",
      "event_date_initiated": "2003-09-05",
      "event_date_posted": "2003-10-15",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-01-29",
      "res_event_number": "26509",
      "k_numbers": [
        "K001400"
      ],
      "product_description": "SONOLINE Antares Diagnostic Ultrasound System.",
      "code_info": "Catalog No. 5936518, 7035415, 5936682, 5936682, 5936708, 5936716, 5936724  Serial numbers:  10106, 10107, 10108, 10253, 10323, 10347, 10352, 10392, 10393, 10394, 10407, 10429, 10430, 10431, 10462, 10465, 10470, 10475, 10492, 10504, 10511, 10535, 10540, 10541, 10542, 10543, 10576, 10585, 10611, 10614, 10626, 10651, 10662, 10712, 10724, 10727, 10745, 10819, 10829, 10837, 10843, 10848, 10849, 10850, 10851, 10852, 10861, 10869, 10873, 10875, 10921, 11008, 11022, 11025, 11049, 11050, 11051, 11053, 11054, 11071, 11102, 11104,  10012, 10027, 10195, 10471, 10483, 10484, 10491, 10583, 10664, 10703, 11033, 11034, 10781, 10432, 10257,  10262, 10274, 10281, 10338, 10383, 10493, 10686, 10836, 10847, 11009, 11030, 11057, 10400, 10401, 10453, 10466, 10737, 10752, 10777, 10778, 10784, 11027, 11028, 11029, 10286, 10602, 10753, 10923, 10018, 10058, 10071, 10116, 10434 , 10668, 10970, 10351, 10697, 10991, 10997, 10277, 10681, 11073, 10130, 10267, 10782, 11002, 11019, 11032, 11072, 10648",
      "firm_fei_number": "3023245",
      "recalling_firm": "Siemens Medical Solutions USA, Inc.",
      "address_1": "22010 SE 51st Street",
      "city": "Issaquah",
      "state": "WA",
      "postal_code": "98029-7298",
      "additional_info_contact": "425-392-9180",
      "reason_for_recall": "Product labeling failed to include complete information about ALARA  (As Low As Reasonably Achievable) safety instructions.",
      "root_cause_description": "Other",
      "action": "On 9/5/03 the firm issued a letter dated September 2003 via overnight delivery.   The letter states that a CD-Rom is included that provides a new manual that is  to replace the previous manual.  The new manual provides information that was previously omitted regarding the ALARA information.",
      "product_quantity": "136 units",
      "distribution_pattern": "The firm distributed units to 37 hospitals and medical centers nationwide. \n\nInternational distribution includes\n\nNo military or government distribution.",
      "openfda": {}
    }
  ]
}