{
  "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": "Waukegan",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93075",
      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "3651 Birchwood Dr",
      "address_2": "N/A",
      "postal_code": "60085-8337",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide distribution to AK, AL, AR, AZ, CA, CO, CT, FL, GA, HI, IA, ID, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, TN, TX, UT, VA, WA, WI, WV, WY.",
      "recall_number": "Z-0149-2024",
      "product_description": "Monoject\" 35 mL Syringe Luer-Lock Tip Soft Pack",
      "product_quantity": "1,097,048 units",
      "reason_for_recall": "Demonstrated recognition and compatibility issues with syringe infusion pumps.",
      "recall_initiation_date": "20230920",
      "center_classification_date": "20231026",
      "report_date": "20231101",
      "code_info": "Product Code: 1183500777;   UDI/DI: 10192253034691 - each, 20192253034698 - box, 50192253034699 - case;    Lot Numbers: 221201, 230201, 230601, 230602"
    }
  ]
}