{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92333",
      "recalling_firm": "Philips North America",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2296",
      "voluntary_mandated": "FDA Mandated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide",
      "recall_number": "Z-1589-2023",
      "product_description": "CombiDiagnost R90 R1.1",
      "product_quantity": "25 systems in total",
      "reason_for_recall": "Philips has identified a compliance issue where ProxiDiagnost N90 R.1.0, CombiDiagnost R90 R.1.0 and CombiDiagnost R90 R1.1 systems are missing a certification label required by the Food and Drug  Administration (FDA).",
      "recall_initiation_date": "20230303",
      "center_classification_date": "20230515",
      "report_date": "20230524",
      "code_info": "REF number: 709031 Serial Number: 10001071, 10001072, 10001086, 10001087, 10001114"
    }
  ]
}