{
  "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": "98154",
      "recalling_firm": "Medline Industries, LP",
      "address_1": "3 Lakes Dr",
      "address_2": "",
      "postal_code": "60093-2753",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution.",
      "recall_number": "Z-1059-2026",
      "product_description": "Medline Kits containing B. Braun IV Administration Sets and Pump Administration Sets, labeled as:    NEURO ANGIO PACK, Medline kit SKU DYNJ38935",
      "product_quantity": "12 units",
      "reason_for_recall": "Medline kits contain B. Braun IV Administration Sets and Pump Administration Sets which were recalled due to customer complaints identifying that the check valve components may become stuck in the open or closed positions.",
      "recall_initiation_date": "20251126",
      "center_classification_date": "20260112",
      "report_date": "20260121",
      "code_info": "UDI/DI 10884389725092 (EA) 40884389725093 (CS), Lot number 25IBC144",
      "more_code_info": ""
    }
  ]
}