{
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    "terms": "https://open.fda.gov/terms/",
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      "event_date_posted": "2007-04-04",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-11-09",
      "res_event_number": "37018",
      "product_code": "LDS",
      "product_description": "ThermaSure Medical Device Drying Cabinet, series 130",
      "code_info": "Catalog #s 090035-00, 090035-03, 090036-00, 090036-02.  Serial Numbers:  350305, 350306, 350307, 350308, 360309, 350310, 350311, 360312, 350313, 350314, 350401, 350402, 350403, 350404, 350405, 350406, 350407, 350408, 350409, 350410, 350411, 350412, 350413, 350414, 350415, 350416, 350417, 350418, 350419, 350420, 350421, 350422, 350423, 350424, 350425, 350426, 350427, 350501, 360502, 350503, 350504, 350505, 350506, 350507, 350508, 350509, 350510, 350511, 350512, 350513, 350514, 350515, 350516, 350517, 350518, 360519, 350520, 350521, 350522, 350523, 350524, 350525, 350526, 350527, 350528, 350529, 350530, 360531, 350532, 350533, 350534, 350601, 350602, 350603, 350604, 350605, 350606, 350607, 350608, 350609, 350610, 360611, 360612, 350613, 350614, 350615, 350616, 350617, 350618, 350619, 350620, 350621, 350621A, 350622, 350623, 350624, 350625, 350626, 350627, 350628, 350629.",
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      "recalling_firm": "Cenorin",
      "address_1": "6324 S 199th Pl Ste 107 6324 S 199th Pl",
      "address_2": "Ste 107",
      "city": "Kent",
      "state": "WA",
      "postal_code": "98032",
      "additional_info_contact": "Beth Robinweiler\n253-395-2400",
      "reason_for_recall": "Potential for user to receive an electrical shock.",
      "root_cause_description": "Other",
      "action": "Letter dated 12/20/2006 notifying customers of potential shock hazard under certain fault conditions and that a corrective action upgrade is being developed.",
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      "distribution_pattern": "Worldwide.",
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