{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97612",
      "recalling_firm": "Philips North America",
      "address_1": "222 Jacobs St",
      "address_2": "",
      "postal_code": "02141-2296",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the states of CA, IA, TN, TX, VA.",
      "recall_number": "Z-0165-2026",
      "product_description": "Cardiac Workstation 5000;   Model Number: 860439;",
      "product_quantity": "28 units",
      "reason_for_recall": "Failure of Environmental Stress Testing from a pinched power module wire within the housing of the Cardiac Workstation device which resulted in a short.",
      "recall_initiation_date": "20250912",
      "center_classification_date": "20251016",
      "report_date": "20251022",
      "code_info": "Model Number: 860439; UDI-DI: 00884838094826; Serial Numbers:",
      "more_code_info": ""
    }
  ]
}