{
  "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": "2026-08-19",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Elkton",
      "state": "MD",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99285",
      "recalling_firm": "Terumo Medical Corporation",
      "address_1": "950 Elkton Blvd",
      "address_2": "",
      "postal_code": "21921-5322",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-2930-2026",
      "product_description": "GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060.    The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.",
      "product_quantity": "7,490 units",
      "reason_for_recall": "Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.",
      "recall_initiation_date": "20260615",
      "center_classification_date": "20260810",
      "report_date": "20260819",
      "code_info": "Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.",
      "more_code_info": ""
    }
  ]
}