{
  "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": "2026-09-03",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "cfres_id": "222029",
      "product_res_number": "Z-2939-2026",
      "event_date_initiated": "2026-07-24",
      "event_date_posted": "2026-08-14",
      "recall_status": "Open, Classified",
      "res_event_number": "99631",
      "product_code": "RCE",
      "product_description": "Lago X",
      "code_info": "All serial numbers.",
      "firm_fei_number": "3002679892",
      "recalling_firm": "Spectral Instruments Inc",
      "address_1": "420 N Bonita Ave",
      "city": "Tucson",
      "state": "AZ",
      "postal_code": "85745-2747",
      "reason_for_recall": "Momentary absence of On-Screen \"X-Ray On\" banner during run readiness check.",
      "root_cause_description": "Radiation Control for Health and Safety Act",
      "action": "Customer notification letters dated August 21, 2023 and allows for scheduling of the software\nupgrade corrections.",
      "product_quantity": "40",
      "distribution_pattern": "United States.",
      "openfda": {
        "device_name": "Cabinet X-Ray, Industrial",
        "medical_specialty_description": "Unknown",
        "regulation_number": "",
        "device_class": "N"
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}