{
  "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": "95301",
      "recalling_firm": "Philips North America",
      "address_1": "222 Jacobs St",
      "address_2": "N/A",
      "postal_code": "02141-2296",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide. Global Distribution.",
      "recall_number": "Z-0007-2025",
      "product_description": "IntelliVue G7m Anesthesia Gas Module, Product Number 866173",
      "product_quantity": "8,449 devices",
      "reason_for_recall": "The 866173 lntelliVue G7m Anesthesia Gas Modules could have a component issue that may trigger an interruption of the gas measurement. This issue concerns the G7m's sample gas pump which could stop working, producing a technical, INOP (inoperable) alarm. The pump may fail prematurely when there is friction caused by an abrasion. This recall is for an IMPORTANT PRODUCT NOTICE dated 1/18/23.",
      "recall_initiation_date": "20230118",
      "center_classification_date": "20241001",
      "report_date": "20241009",
      "code_info": "UDI-DI: 00884838051492; Serial Numbers: DE43800129 through DE43812627"
    }
  ]
}