{
  "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": "2026-08-20",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "50292",
      "product_res_number": "Z-0687-2007",
      "event_date_initiated": "2007-01-24",
      "event_date_posted": "2007-03-31",
      "recall_status": "Terminated",
      "event_date_terminated": "2007-12-12",
      "res_event_number": "37291",
      "product_code": "MNB",
      "pma_numbers": [
        "P000040"
      ],
      "product_description": "HTA Console  System, 110 Volt, Product Number: 56000  (HTA system is a software-controlled hysteroscopic thermal endometrial ablation system)",
      "code_info": "Unit Numbers: N1190JC, N1191JC, N1192JC, N1194JC, N1197JC, N1199JC, N1200JC, N1201JC, N1203JC, N1204JC, N1205JC, N1206JC, N1208JC, N1210JC, N1211JC, N1214JC, N1215JC, N1217JC, N1218JC, N1220JC, N1222JC, N1226JC, N1227JC, N1229JC, N1230JC, N1231JC, N1232JC, N1233JC, N1234JC, N1235JC, N1237JC, N1238JK, N1239JF, N1240JF, N1241JF, N1242JF, N1243JF, N1245JF, N1247JF, N1251JF, N1252JF, N1253JF, N1254JF, N1255JF, N1257JF, N1258JF, N1259JF, N1261JF, N1262JF, N1263JF, N1264JF, N1266JF, N1267JF, N1268JF, N1269JF, N1294JI, N1295JI,",
      "firm_fei_number": "3001451463",
      "recalling_firm": "Boston Scientific Corporation",
      "address_1": "One Boston Scientific Place",
      "city": "Natick",
      "state": "MA",
      "postal_code": "01760-1536",
      "additional_info_contact": "Cindy Finney\n508-683-4186",
      "reason_for_recall": "Defective integrated circuit board could result in loss of the system pump and patient injury (hot fluid 90 degree C into uterus) if in use during the recirculation/heating phase of treatment",
      "root_cause_description": "Other",
      "action": "Boston Scientific notiifed accounts by letter dated January 24, 2007 via federal Express Mail. Accounts were requested to examine inventory, remove and return product.",
      "product_quantity": "57 units",
      "distribution_pattern": "Worldwide-USA, UK, Denmark, Italy, and France",
      "openfda": {
        "pma_number": [
          "P160047",
          "P010013",
          "P140013",
          "P020031",
          "P000032",
          "P000040",
          "P180032",
          "P970021",
          "P230002"
        ],
        "registration_number": [
          "1834003",
          "3008468035",
          "3012018285",
          "3006330030",
          "3011011193",
          "2954783",
          "3043236281",
          "3024021261",
          "2031093",
          "3010273872",
          "3009327445",
          "1220477",
          "1222780",
          "3017196117",
          "2030624",
          "2953359",
          "3010034260",
          "3007200016",
          "1222928"
        ],
        "fei_number": [
          "3003186357",
          "3008468035",
          "3012018285",
          "3006330030",
          "3011011193",
          "3001236549",
          "3043236281",
          "3024021261",
          "1000120743",
          "3000215205",
          "1000120613",
          "3010273872",
          "3009327445",
          "3000206435",
          "1220477",
          "3017196117",
          "1000139922",
          "3010034260",
          "3007200016"
        ],
        "device_name": "Device, Thermal Ablation, Endometrial",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "3"
      }
    }
  ]
}