{
  "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": "83271",
      "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": "Letter",
      "distribution_pattern": "Distribution in the US to Texas.  International distribution to France, Greece and Switzerland.",
      "recall_number": "Z-1965-2019",
      "product_description": "Repair RIC5-9A-RS System, imaging, pulsed doppler, ultrasonic and Refurbish RIC-5-9-D REALTIME 4D",
      "product_quantity": "2 devices",
      "reason_for_recall": "Potential for a transducer mis-alignment in certain transvaginal probes.",
      "recall_initiation_date": "20190702",
      "center_classification_date": "20190712",
      "termination_date": "20201005",
      "report_date": "20190724",
      "code_info": "Model H48701EJ; Serial Number 205375KR9; (UDI Number) 01008406821085531116071121205375KR9.      Model KTZ157043-R   Serial Number 152323KR2 (UDI Number   Not Available)"
    }
  ]
}