{
  "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": "2026-08-13",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "25815",
      "product_res_number": "Z-0299-03",
      "event_date_initiated": "2003-01-22",
      "event_date_posted": "2003-04-03",
      "recall_status": "Terminated",
      "event_date_terminated": "2004-02-05",
      "res_event_number": "25428",
      "product_description": "Biosound Caris Plus Ultrasound System with phased array probes, model 7230.\nBiosound Megas Ultrasound System with phased array probes, model 7250",
      "code_info": "All Caris Plus units with PA220, PA121, PA122, PA023 or PA230 probes. All Megas units with PA122 or PA023 probes.",
      "firm_fei_number": "1826555",
      "recalling_firm": "Biosound Esaote, Inc.",
      "address_1": "8000 Castleway Drive",
      "city": "Indianapolis",
      "state": "IN",
      "postal_code": "46250",
      "additional_info_contact": "Thomas B. Feick\n317-813-6006",
      "reason_for_recall": "Excessive power output due to a faulty voltage controller.",
      "root_cause_description": "Other",
      "action": "This is a professional use device, and service upgrade notices were issued to customers on or about 1/22/03 informing them that the firm will be contacted by a service representative to schedule a software upgrade.",
      "product_quantity": "157 Caris Plus systems, 503 Megas",
      "distribution_pattern": "United States and Canada",
      "openfda": {}
    }
  ]
}