{
  "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": "93676",
      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "3651 Birchwood Dr",
      "address_2": "",
      "postal_code": "60085-8337",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US nationwide and Canada.  Foreign distribution updated 9/6/2024 to only include Canada.",
      "recall_number": "Z-0854-2024",
      "product_description": "Cardinal Health Monoject, 12 mL Syringe Luer-Lock Tip  Soft Pack, REF 1181200777T",
      "product_quantity": "",
      "reason_for_recall": "Cardinal Health is expanding their previous product correction actions to a product removal of all sizes of Cardinal Health brand Monoject sterile Syringe Luer-Lock (1, 3, 6, 12, 20, 35, and 60 mL) and Cardinal Health brand Monoject sterile Enteral Syringes with the ENFit connection (1, 3, 6, 12, 35, and 60 mL) due to a change in manufacturing and rebranding efforts.",
      "recall_initiation_date": "20231228",
      "center_classification_date": "20240202",
      "report_date": "20240214",
      "code_info": "UDI/DI 50192253025819 (Case), 20192253025818 (Box), 10192253025811 (Each), Lot Numbers:  221101, 221102, 221103, 221104",
      "more_code_info": ""
    }
  ]
}