{
  "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": "93342",
      "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": "United States Territories of Puerto Rico, Guam, and Virgin Islands",
      "recall_number": "Z-0227-2024",
      "product_description": "Integris-Allura IGTS Fixed Systems",
      "product_quantity": "",
      "reason_for_recall": "Philips has become aware of an issue with the Philips Integris-Allura, Allura Xper and Azurion systems that have been delivered to Puerto Rico without a warning label and the Source-to-Skin Distance Spacer (Tube-spacer) is missing.",
      "recall_initiation_date": "20231004",
      "center_classification_date": "20231109",
      "report_date": "20231115",
      "code_info": "INTEGRIS Allura 15-12 (mono) 68",
      "more_code_info": ""
    }
  ]
}