{
  "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": "2026-06-24",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Chesterfield",
      "state": "MO",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98660",
      "recalling_firm": "Katalyst Surgical, LLC",
      "address_1": "722 Goddard Ave",
      "address_2": "",
      "postal_code": "63005-1100",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France.",
      "recall_number": "Z-2069-2026",
      "product_description": "DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23",
      "product_quantity": "5 units",
      "reason_for_recall": "Field Safety Corrective Action for IFU in DEX Forceps and Scissors.",
      "recall_initiation_date": "20260325",
      "center_classification_date": "20260506",
      "report_date": "20260513",
      "code_info": "Lot Code: Model No: DVF4005-23 UDI-DI: (01)10817489021658(11)250924(17)280924(10)M50529 Lot Number: M50529 Expiration Date: 09/04/2028",
      "more_code_info": ""
    }
  ]
}