{
  "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": "2026-09-05",
    "results": {
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      "product_res_number": "Z-1347-2021",
      "event_date_initiated": "2021-01-19",
      "event_date_created": "2021-04-02",
      "recall_status": "Completed",
      "res_event_number": "87281",
      "product_code": "LZH",
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      "recalling_firm": "Cardinal Health 200, LLC",
      "address_1": "3651 Birchwood Dr",
      "city": "Waukegan",
      "state": "IL",
      "postal_code": "60085-8337",
      "reason_for_recall": "The potential for air appearing in the enteral feed pumping set tubing during set-up.",
      "root_cause_description": "Process control",
      "action": "On 03/01/2021, Cardinal Health issued an Urgent Medical Device Correction notice to customers via letter to the potential of air entering the feed set tubing of enteral fusion pumps with the specified product codes",
      "product_quantity": "146,944,334 units",
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        "device_name": "Pump, Infusion, Enteral",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5725",
        "device_class": "2"
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}