{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93767",
      "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": "Domestic distribution nationwide. International distribution worldwide.",
      "recall_number": "Z-0930-2024",
      "product_description": "BrightView X, gamma camera for SPECT;    Model Nos.:    6-digit format 882478;  12-digit format 453560824741  453560829261;",
      "product_quantity": "56 US; 46 OUS",
      "reason_for_recall": "Detector may unexpectedly fall due to a component failure. If the detector is positioned below center of gantry, there is a potential for abrasion, contusion, laceration, and/or fracture to the patient's lower limbs, as well as an interruption to normal system operation. If detector is positioned above center of gantry, there may be an interruption to normal system operation.",
      "recall_initiation_date": "20231215",
      "center_classification_date": "20240202",
      "report_date": "20240214",
      "code_info": "All serial numbers are affected.  No UDI-DI available for this product.",
      "more_code_info": ""
    }
  ]
}