{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Saint Charles",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98255",
      "recalling_firm": "Vortex Surgical Inc.",
      "address_1": "4 Research Park Dr Ste 124",
      "address_2": "N/A",
      "postal_code": "63304-5639",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL, HI, IA, IL, IN, KY, MA, MI, MN, MS, NC, NE, NJ, NM, NY, OH, OR, PA, RI, SC, SD, TN, TX, WA, WI, VA; and OUS (foreign) to countries of: Australia, Chile, China, France, Germany, India, Ireland, Italy, Japan, Korea, Mexico, Netherlands, Philippines, Poland, Puerto Rico, Spain, Switzerland, Taiwan, United Kingdom, Vietnam.",
      "recall_number": "Z-1254-2026",
      "product_description": "Vortex Surgical TID Pharos Illuminated Depressor, VS0801B",
      "product_quantity": "14,789 (8651 US; 6138 OUS)",
      "reason_for_recall": "XXX",
      "recall_initiation_date": "20251216",
      "center_classification_date": "20260204",
      "report_date": "20260211",
      "code_info": "Pouch UDI 810123481309 Box UDI 810123481712 Lot 2403027R"
    }
  ]
}