{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Northfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "97495",
      "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": "E-Mail",
      "distribution_pattern": "US Distribution to States of: FL, MD, NJ, TN",
      "recall_number": "Z-2592-2025",
      "product_description": "Sterile Medline Convenience Kits:  1) MAJOR PACK L-F, Model Number: DYNJ0382730O;   2) LB BASIC CUSTOM PACK, Model Number: DYNJ61038B",
      "product_quantity": "22 units",
      "reason_for_recall": "Convenience kits labeled as sterile have not gone through the sterilization process.",
      "recall_initiation_date": "20250808",
      "center_classification_date": "20250926",
      "report_date": "20251008",
      "code_info": "1) DYNJ0382730O, UDI-DI: 10198459117992(each), 40198459117993(case), Lot Number: 25GBC583; 2) DYNJ61038B, UDI-DI: 10195327596316(each), 40195327596317(case), Lot Number: 25GBF720;"
    }
  ]
}