{
  "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": "Melbourne",
      "address_1": "3275 Suntree Blvd",
      "reason_for_recall": "Has a Potential Pinch Hazard to user performing Machine QA in an MRI environment.",
      "address_2": "",
      "product_quantity": "6 Units.",
      "code_info": "Serial #'s: 92327001, 92327002, 92327003, 84118005, 84118006, 84118004, 84118001, 84118002, and 84118003",
      "center_classification_date": "20150113",
      "distribution_pattern": "Distributed in the states of CA, CO, and OH.",
      "state": "FL",
      "product_description": "IC PROFILER-MR - Model 1123.    A radiologic quality assurance instrument is a device intended for medical purposes to measure a physical characteristic associated with another radiologic device.",
      "report_date": "20150121",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Sun Nuclear Corporation",
      "recall_number": "Z-0959-2015",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "product_type": "Devices",
      "event_id": "69751",
      "termination_date": "20150323",
      "more_code_info": "",
      "recall_initiation_date": "20140808",
      "postal_code": "32940-7514",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}