{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Waukesha",
      "state": "WI",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "77287",
      "recalling_firm": "GE Healthcare, LLC",
      "address_1": "3000 N Grandview Blvd",
      "address_2": "N/A",
      "postal_code": "53188-1615",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Worldwide Distribution - USA (nationwide)  Distribution.",
      "recall_number": "Z-2323-2017",
      "product_description": "Infant Warmer System (IWS)",
      "product_quantity": "34986",
      "reason_for_recall": "GE Healthcare  has recently become aware of a potential safety issue related to loose screws in the \u001cHeater Head\u001d of the Infant Warmer System (IWS).   Hot screws from the \u001cHeater Head\u001d of the IWS could fall onto  the  bed  if the  \u001cHeater Head\u001d assembly  has  been improperly  serviced. This situation can be clinically hazardous because thermal injury to a   patient could result. Two injuries have been reported as a result of this issue.",
      "recall_initiation_date": "20170505",
      "center_classification_date": "20170609",
      "termination_date": "20180712",
      "report_date": "20170621",
      "code_info": "Medical device listing number: D103053, D103054, D103056, D103057, D183529"
    }
  ]
}