{
  "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": "96374",
      "recalling_firm": "MEDLINE INDUSTRIES, LP - Northfield",
      "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": "Worldwide distribution - US Nationwide and the country of Canada.",
      "recall_number": "Z-1453-2025",
      "product_description": "Medline procedure kits labeled as:    1) C SCOPE DISPOSABLE KIT, Pack Number 613034700,   2) C SCOPE DISPOSABLE KIT, Pack Number 613034702",
      "product_quantity": "90 units",
      "reason_for_recall": "Medical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/other quality issues have been identified that may pose a risk to patient health.",
      "recall_initiation_date": "20250211",
      "center_classification_date": "20250325",
      "report_date": "20250402",
      "code_info": "1) Pack Number 613034700:  UDI/DI 10850009724004 (each) 40850009724005 (case), Lot Number 613034700;  2) Pack Number 613034702:  UDI/DI 10850009724066 (each) 40850009724067 (case), Lot Number 613034702"
    }
  ]
}