{
  "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": "2026-05-06",
    "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": "61877",
      "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": "6 US customers",
      "recall_number": "Z-1821-2012",
      "product_description": "Philips Easy Diagnost    Product Usage:  Stationary Fluoroscopic system",
      "product_quantity": "6",
      "reason_for_recall": "If a lead ruler is not positioned in the same plane as the anatomical image detail to be measured, measured object distances (using the ruler) can be wrong by a corresponding factor. If, additionally, the measurement tool is not used to check the ruler, or is used in the right way (ie: calibration), such calibration error is not detected.  As a result of this, a surgical intervention may be execut",
      "recall_initiation_date": "20120511",
      "center_classification_date": "20120618",
      "termination_date": "20161006",
      "report_date": "20120627",
      "code_info": "All systems with Eleva software version 4.x and stitching option."
    }
  ]
}