{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Minnetonka",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94613",
      "recalling_firm": "St. Jude Medical",
      "address_1": "14901 Deveau Pl",
      "address_2": "",
      "postal_code": "55345-2126",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US and Canada",
      "recall_number": "Z-2348-2024",
      "product_description": "St. Jude Medical Agilis NxT Steerable Introducer, REF 408309",
      "product_quantity": "129 units",
      "reason_for_recall": "One lot of product has dilators that are too short and will not extend outside the introducer sheath.",
      "recall_initiation_date": "20240430",
      "center_classification_date": "20240712",
      "report_date": "20240724",
      "code_info": "UDI/DI 05414734206099, Lot Number 10071090",
      "more_code_info": ""
    }
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}