{
  "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": "98226",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "N/A",
      "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.",
      "recall_number": "Z-1195-2026",
      "product_description": "Medline medical procedure convenience kits labeled as:    1) INPATIENT CTRL LN DRG CHG, Kit SKU DT22880;   2) ADULT CVC DRSG CHG W/ADHESIVE, Kit SKU DYNDC3283A.",
      "product_quantity": "1,928 total",
      "reason_for_recall": "Medline kits were manufactured and distributed containing MASTISOL liquid adhesive which was recalled due to complaints that the butyrate tubing cracked during actuation of the vials of MASTISOL Liquid Adhesive.",
      "recall_initiation_date": "20251212",
      "center_classification_date": "20260128",
      "report_date": "20260204",
      "code_info": "Medline Kit SKU DT22880:  UDI/DI 10653160995470 (EA) 40653160995471 (CS), Lot Number 25KMJ441;  Medline Kit SKU DYNDC3283A:  UDI/DI 10198459313240 (EA) 40198459313241 (CS), Lot Number 25KMH515."
    }
  ]
}