{
  "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": "2026-06-24",
    "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": "98664",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Worldwide distribution.",
      "recall_number": "Z-2009-2026",
      "product_description": "Medline medical procedure kits, containing Medline Neuro Sponges, labeled as follows:  PEDS AIRWAY PACK, Medline Kit Number SKU DYNJ86657A",
      "product_quantity": "306 kits",
      "reason_for_recall": "During an internal review, Medline identified higher-than-expected endotoxin levels on a representative Medline neuro sponge product, indicating that in-market product may be out-of-specification for endotoxin.",
      "recall_initiation_date": "20260319",
      "center_classification_date": "20260430",
      "report_date": "20260506",
      "code_info": "Medline Kit Number SKU DYNJ86657A:  UDI/DI each 10198459431678, UDI/DI case 40198459431679, Lot Numbers:  26ABM977, 25KBM387, 25IBG995, 25GBW704.",
      "more_code_info": ""
    }
  ]
}