{
  "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": "98951",
      "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": "US Nationwide distribution. OUS distribution pending.",
      "recall_number": "Z-2435-2026",
      "product_description": "Medline convenience kits:    BASIC EYE  DYNJ905154I    TUBAL LIGATION CDS  CDS760053K",
      "product_quantity": "49,654 kits total",
      "reason_for_recall": "Kits contain recalled lot of Ferndale Laboratories MASTISOL Liquid Adhesive. Butyrate tubing may crack during actuation and render product unusable for application.",
      "recall_initiation_date": "20260427",
      "center_classification_date": "20260612",
      "report_date": "20260624",
      "code_info": "DYNJ905154I UDI-DI 10198459549977 lots 26ABB308 26BBA671  CDS760053K UDI-DI 10195327182977 lot 25KBP010",
      "more_code_info": ""
    }
  ]
}