{
  "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": "2026-08-15",
    "results": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "cfres_id": "189294",
      "product_res_number": "Z-0147-2022",
      "event_date_initiated": "2021-09-08",
      "event_date_created": "2021-10-19",
      "recall_status": "Terminated",
      "event_date_terminated": "2023-10-13",
      "res_event_number": "88687",
      "product_code": "PEZ",
      "product_description": "Kit: Central Line Dres Change 20/Cs",
      "code_info": "Product Code: 59815B, Batch 0000285665; Kit expiration date 03/31/2024  UDI: 20809160170523",
      "firm_fei_number": "1030451",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "city": "Arden",
      "state": "NC",
      "postal_code": "28704-9302",
      "reason_for_recall": "The ChloraPrep 3ml kit component has a shorter expiry date than the labeled kit expiry date.",
      "root_cause_description": "Process control",
      "action": "A customer email was sent to the impacted distributor dated 09/16/2021.  The distributor was notified of the recall issue and instructed to inventory and segregate affected product.  Warning labels were provided and are to be affixed to the affected kits.  Relabeling should be conducted in a manner that does not allow other pertinent labeling information to be covered up.  The distributor was also notified that the recall should be carried out to the end user level.",
      "product_quantity": "42 cases",
      "distribution_pattern": "Distribution to a single US distributor in Michigan",
      "openfda": {
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        ],
        "device_name": "Central Venous Catheter Dressing Change Kit",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5200",
        "device_class": "2"
      }
    }
  ]
}