{
  "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": "2026-04-29",
    "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": "98529",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution in the state of MN.",
      "recall_number": "Z-1693-2026",
      "product_description": "Sterile Radiology Procedure Kits, Model Number DYNDH1491B",
      "product_quantity": "420 units",
      "reason_for_recall": "There is a potential breach in the sterile pouch packaging for one lot of radiology kits, which may compromise product sterility.",
      "recall_initiation_date": "20260218",
      "center_classification_date": "20260327",
      "report_date": "20260408",
      "code_info": "UDI-DI: (CS) 40198459071455, (EA) 10198459071454; Lot Number: 25GBB924",
      "more_code_info": ""
    }
  ]
}