{
  "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": "91195",
      "recalling_firm": "Philips North America Llc",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2289",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide.",
      "recall_number": "Z-0462-2023",
      "product_description": "Philips MR 7700 System, Model Number 782120",
      "product_quantity": "566 total",
      "reason_for_recall": "Gradient Coil may act as a heat source with a potential to produce smoke and/or fire.",
      "recall_initiation_date": "20221122",
      "center_classification_date": "20221208",
      "report_date": "20221214",
      "code_info": "Model 782120: UDI-DI: 00884838104112; Serial Numbers: 65005 65006 65007 65008"
    }
  ]
}