{
  "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": "2026-09-23",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "99667",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in states of Arkansas, Florida, North Carolina, Maryland, and Texas.",
      "recall_number": "Z-3208-2026",
      "product_description": "Convenience kits    MINOR PACK\t  \tDYNJ58421A  \t  SPRINGHILL MINOR PACK\t  \tDYNJ40734F",
      "product_quantity": "459",
      "reason_for_recall": "Kits may exhibit open seals in sterile pouch packaging. Open seal may compromise product sterility. If not detected prior to use, issue may lead to contamination of sterile field or patient infection if product is used.",
      "recall_initiation_date": "20260731",
      "center_classification_date": "20260916",
      "report_date": "20260923",
      "code_info": "DYNJ58421A    UDI-DI 10193489970487    Lot 25HBQ049          DYNJ40734F    UDI-DI 10198459162084    Lots 25GBO299   25IBS607",
      "more_code_info": ""
    }
  ]
}