{
  "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": "64902",
      "recalling_firm": "Philips Healthcare Inc.",
      "address_1": "3000 Minuteman Road",
      "address_2": "N/A",
      "postal_code": "01810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide (AR, AZ, CA, DE, FL, GA, IA, IL, IN, KS, MD, MI, MN, NC, NM, NY, OH, OR, PA, SC, TX, VT, WI)",
      "recall_number": "Z-1706-2017",
      "product_description": "Mobile Diagnostic X-Ray System with Digital Panel",
      "product_quantity": "220 systems",
      "reason_for_recall": "When the operator moves an image to another view then the electronic marker might be placed at the wrong anatomical position in the resulting image.",
      "recall_initiation_date": "20121128",
      "center_classification_date": "20170404",
      "termination_date": "20180531",
      "report_date": "20170412",
      "code_info": "*** All units ***"
    }
  ]
}