{
  "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-0850-2024",
      "product_description": "Cardinal Health Monoject, 60mL Enteral Syringe (purple) -  For Use with ENFit Connection System, REF 460SE",
      "product_quantity": "397676 units",
      "reason_for_recall": "The listed lots of Cardinal Health Monoject Enteral Syringes with ENFit (6, 12, 35, 60 mL) have recognition and compatibility issues with certain syringe enteral feeding pumps.  As a result, Cardinal Health recommends that they not be used with enteral syringe feeding pumps.",
      "recall_initiation_date": "20231228",
      "center_classification_date": "20240202",
      "report_date": "20240214",
      "code_info": "UDI/DI 26971564466251 (Case), 16971564466254 (Box), 06971564466257 (Each), Lot Numbers:  230501, 230701 and 230702",
      "more_code_info": ""
    }
  ]
}