{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Tustin",
      "address_1": "2441 Michelle Dr",
      "reason_for_recall": "The firm initiated this recall of certain Toshiba Diagnostic Ultrasound Systems because it has been found that under certain conditions, the temperature of the transducer head may increase in 2D+PW mode or 2D+CDI (POWER, ADF) +PW mode. When the system is used under both conditions listed below, the temperature of the transducer head connected to the system may increase in temperature and possibly",
      "address_2": "P.O. Box 2068",
      "product_quantity": "427 units (1352 total)",
      "code_info": "Lot Numbers not utilized.  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      "center_classification_date": "20131030",
      "distribution_pattern": "Nationwide Distribution including and US Territory Puerto Rico",
      "state": "CA",
      "product_description": "Aplio MX Diagnostic Ultrasound System SSA-780A    Used for routine diagnostic imaging",
      "report_date": "20131106",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Toshiba American Medical Systems Inc",
      "recall_number": "Z-0121-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "66059",
      "termination_date": "20160628",
      "recall_initiation_date": "20130805",
      "postal_code": "92780-7047",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}