{
  "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": "93560",
      "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": "Distribution was made to MD, OH, TN, TX, and WI.  There was no government/military/foreign distribution.",
      "recall_number": "Z-0711-2024",
      "product_description": "Medline Gown Poly W/Breath Sleeves XL AAMIK Level 4 (Eclipse gown), REF SPT-2208CS, 100/pack, Non-Sterile.",
      "product_quantity": "2,100 gowns",
      "reason_for_recall": "Surgical gowns were manufactured with the wrong sleeve.",
      "recall_initiation_date": "20231129",
      "center_classification_date": "20240111",
      "report_date": "20240117",
      "code_info": "Lot #11023060120, UDI (01)40080196029755(11)230615(10)11023060120.",
      "more_code_info": ""
    }
  ]
}