{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Gilbert",
      "state": "AZ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92719",
      "recalling_firm": "PARAGON VISION SCIENCES, Inc",
      "address_1": "2120 W Guadalupe Rd Ste 112",
      "address_2": "N/A",
      "postal_code": "85233-2810",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide distribution including in the states of AK, AL, AR, \tAZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, ME, MI, MN, MO, MS, MT, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, PR, RI, SC, SD, TN, TX, UT, VA, VT, WA,\tWI, WV and the countries of Australia, Canada, China, Japan, Vietnam.",
      "recall_number": "Z-2516-2023",
      "product_description": "Fargo Ortho-K Lens",
      "product_quantity": "18,820 lenses",
      "reason_for_recall": "Manufactured lenses are not covered by existing FDA approval",
      "recall_initiation_date": "20230626",
      "center_classification_date": "20230905",
      "report_date": "20230913",
      "code_info": "All Lots, DI - B22208"
    }
  ]
}