{
  "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": "74685",
      "recalling_firm": "Philips Electronics North  America Corporation",
      "address_1": "3000 Minuteman Rd",
      "address_2": "N/A",
      "postal_code": "01810-1032",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution to the states of : ME, NE, OR, CA, TX, NC, WA and OH.",
      "recall_number": "Z-2682-2016",
      "product_description": "Philips DuraDiagnost stationary X-ray system",
      "product_quantity": "15",
      "reason_for_recall": "Buttons or keys on the monitor allow the user to turn the volume setting down to \u001c0\", in which case the beep will not be heard at the conclusion of an exposure, as required 21 CFR 1020.31(j), and the Height-Adjustable Tabletop is missing the required labels [21 CFR 1010.2., 21 CFR 1010.3(a), and 21 CFR 1020.30(3)].",
      "recall_initiation_date": "20150917",
      "center_classification_date": "20160901",
      "termination_date": "20170831",
      "report_date": "20160907",
      "code_info": "SN:  140054  140059  150013  150014  150039  150041  150042  150052  150053  150055  150056  150059  150061  150091  150093"
    }
  ]
}