{
  "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": {
      "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": "92486",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "N/A",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the country of Panama.",
      "recall_number": "Z-2131-2023",
      "product_description": "MEDLINE NON-STERILE PVP SOLUTION, STERILE PACKAGING REF DYNDA2232A",
      "product_quantity": "183240 units",
      "reason_for_recall": "Affected product lots were mislabeled as \"STERILE PVP SLN\" when they should have been titled \"NON-STERILE PVP SOLUTION, STERILE PACKAGING\".",
      "recall_initiation_date": "20230518",
      "center_classification_date": "20230712",
      "report_date": "20230719",
      "code_info": "GTIN 10889942851850, Batch Numbers:  2023011090, 2023011190, 2023011790, 2023012090, 2023012590, 2023020790, 2023022390, 2023022490",
      "more_code_info": ""
    }
  ]
}