{
  "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": [
    {
      "status": "Terminated",
      "city": "Andover",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "67859",
      "recalling_firm": "Philips Medical Systems, Inc.",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide: US:  AL, AR, AZ, CA, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, MA, MD, ME, MN, MO, MS, MT, NC, ND, NH, NJ, NM, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VT, WY / Worldwide including Canada & Mexico",
      "recall_number": "Z-1503-2014",
      "product_description": "Digital Diagnost, stationary radiographic system; Models:  712020/22/25/26/50/52/54/55/57/60/62/80/81/82/85",
      "product_quantity": "985 devices",
      "reason_for_recall": "The footboard of Patient support for stitching can be fixed in upper position.  When the fix clamp (hook) is not correctly adjusted into its correct position, the footboard is not securely held.",
      "recall_initiation_date": "20140317",
      "center_classification_date": "20140424",
      "termination_date": "20200916",
      "report_date": "20140430",
      "code_info": "Units distributed from November 2006 through March 2014.",
      "more_code_info": ""
    }
  ]
}