{
  "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": "Andover",
      "address_1": "3000 Minuteman Road",
      "reason_for_recall": "Values of fluoroscopy time, Air Kerma Rate and  Cumulated Air Kerma may not be displayed \"at  the fluoroscopist's working position\" as per 21 CFR 1003.21",
      "address_2": "",
      "product_quantity": "16 units",
      "code_info": "Serial Numbers:  10110770  11030805  11070848  11070845  11070849  11030806  11090864  11110900  12020982  114087  12030999  12061020  12041003  12061014  12061018  12081040    :",
      "center_classification_date": "20130128",
      "distribution_pattern": "US Nationwide Distribution including the states of AL, CA, CO, CT, IL, MD, MI, MO, NY,  OH, PA",
      "state": "MA",
      "product_description": "Juno DRF , X-ray system, diagnostic, Fluoroscopic, general-purpose  Model: 70920    Product Usage:  Universal R/F, general use",
      "report_date": "20130206",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Philips Healthcare Inc.",
      "recall_number": "Z-0702-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "63868",
      "termination_date": "20170124",
      "more_code_info": "",
      "recall_initiation_date": "20121213",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}