{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87039",
      "recalling_firm": "PHILIPS HOME HEALTHCARE SOLUTION",
      "address_1": "222 Jacobs St",
      "address_2": "",
      "postal_code": "02141-2289",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "Z-0727-2021",
      "product_description": "ProxiDiagnost N90 Image-intensified fluoroscopic x-ray system",
      "product_quantity": "91",
      "reason_for_recall": "After the user selects the Lock-in command, the kV and mA values are not locked immediately and can adjust if the collimator shutter position is changed directly after the Lock-in command.",
      "recall_initiation_date": "20201208",
      "center_classification_date": "20201231",
      "termination_date": "20240621",
      "report_date": "20210203",
      "code_info": "Pending",
      "more_code_info": ""
    }
  ]
}