{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Cambridge",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "87427",
      "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": "E-Mail",
      "distribution_pattern": "US Virgin Island  Foreign:  Australia  Bolivia  China  Germany  Hungary  Indonesia  Italy  Japan  Korea  Korea, Republic of  Latvia  Palestine  Philippines  Romania  Russian Federation  Senegal  Thailand  Uzbekistan",
      "recall_number": "Z-1265-2021",
      "product_description": "Incisive CT Computed Tomography X-ray System  Model: 728143",
      "product_quantity": "105 units (1 US and 104 OUS)",
      "reason_for_recall": "Actuators in the Incisive gantry could result in the gantry failure to self-lock if both of the 2 sides actuators fail. In some cases in systems with affected components, the gantry may tilt forward slowly, in a worst case, reaching to the tilt limit angle +31degrees",
      "recall_initiation_date": "20210222",
      "center_classification_date": "20210316",
      "termination_date": "20230209",
      "report_date": "20210324",
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