{
  "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-2419-2026",
      "product_description": "Medline convenience kits:    INPATIENT CENTRAL LN DRSG KIT  DYNDC3525    PICC/CVC/MIDLINE DRSG CHG KIT  DT13191A    PORT A CATH  CDS982047S    VEIN ABLATION PACK  DYNJ62889C",
      "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": "DYNDC3525 UDI-DI 10198459576294 Lot 25KBM985  DT13191A UDI-DI 10653160998914 Lot 26AMA168  CDS982047S UDI-DI 10198459385735 Lot 26AMB202  DYNJ62889C UDI-DI 10198459416453 Lot 26AMA584",
      "more_code_info": ""
    }
  ]
}