{
  "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-2417-2026",
      "product_description": "MINOR CATH LAB PACK  DYNJ84775A    OR VASCULAR ANGIO PACK  DYNJ47269D    PORT-A-CATH  DYNJ63276G",
      "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": "DYNJ84775A UDI-DI 10195327606527 lot  25LMH070   DYNJ47269D UDI-DI 10195327674786 lot 25LMJ234  DYNJ63276G UDI-DI 10198459458835 lot 26BBC598",
      "more_code_info": ""
    }
  ]
}