{
  "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": "2026-04-15",
    "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": "74083",
      "recalling_firm": "Philips Healthcare",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "USA (nationwide) Distribution to the states of :   ( DuraDiagnost) to the states of :  OH, CA, WA and NE.    (DigitalDiagnost) to the states of : AK, AZ, AL, CA, CT, CO, DE, FL, GA, HI, ID, KY, LA, MA, MN, MD, MS, ME, MO, NE, NY, ND, OH and PA.",
      "recall_number": "Z-1695-2016",
      "product_description": "Philips Healthcare DigitalDiagnost stationary X-ray system",
      "product_quantity": "160",
      "reason_for_recall": "The detector may signal that it is ready for acquisition  when it actually is not, resulting in failure to properly acquire the X-ray image.",
      "recall_initiation_date": "20151110",
      "center_classification_date": "20160603",
      "termination_date": "20170503",
      "report_date": "20160615",
      "code_info": "software version - 4.0.4,  4.1.2,  4.1.3."
    }
  ]
}