{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Minneapolis",
      "state": "MN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90552",
      "recalling_firm": "Medtronic Inc",
      "address_1": "710 Medtronic Pkwy Mailstop Ls245",
      "address_2": "N/A",
      "postal_code": "55432-5603",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1483-2022",
      "product_description": "Medline Sprinter OTW, Model/Catalog Number SPR2512W; The Sprinter Over-the-Wire balloon dilatation catheter has a coaxial shaft with a balloon mounted on its distal tip.",
      "product_quantity": "84 units",
      "reason_for_recall": "Luer has balloon diameter printed as \"2.25mmx12mm\" instead of the correct diameter, \"2.5mmx12mm\" as reflected on the product outer packaging.",
      "recall_initiation_date": "20220624",
      "center_classification_date": "20220801",
      "report_date": "20220810",
      "code_info": "GTIN/UPN 00643169850491, Lot Number:  222066656 Expiration Date: 04/13/2023"
    }
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}