{
  "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": "2026-09-02",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Lexington",
      "state": "MA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99529",
      "recalling_firm": "FUJIFILM Healthcare Americas Corporation",
      "address_1": "81 Hartwell Ave Ste 300",
      "address_2": "N/A",
      "postal_code": "02421-3160",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of NY, VA, KS, OR, OH, and the country of Australia.",
      "recall_number": "Z-3030-2026",
      "product_description": "FUJIFILM Synapse PACS software v7.4.310; radiological  image processing system",
      "product_quantity": "6 units",
      "reason_for_recall": "Software issue may cause the ruler measurement to be inaccurate.",
      "recall_initiation_date": "20260722",
      "center_classification_date": "20260826",
      "report_date": "20260902",
      "code_info": "UDI (01)00854904006008(10)0704310, Serial Numbers:  CV-00272120, CV-0080080176, CV-01318490, CV-01-80102732, CV-80057523, CV-00494020-38"
    }
  ]
}