{
  "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 II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "95843",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "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.",
      "recall_number": "Z-0760-2025",
      "product_description": "RUMMELL, Medline Item No. ST006ST",
      "product_quantity": "21,440 total",
      "reason_for_recall": "Weak seals may result in a breach of sterility, which may not be detectable to the user. This can lead to increased risk of contamination and infection.",
      "recall_initiation_date": "20241112",
      "center_classification_date": "20241223",
      "report_date": "20250101",
      "code_info": "UDI: 10653160251224 (ea) 00653160251227 (case); Lot 2023111490",
      "more_code_info": ""
    }
  ]
}