{
  "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": "2026-08-22",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "cfres_id": "196624",
      "product_res_number": "Z-0464-2023",
      "event_date_initiated": "2022-10-12",
      "event_date_posted": "2022-12-08",
      "recall_status": "Terminated",
      "event_date_terminated": "2025-03-25",
      "res_event_number": "91065",
      "product_code": "OWL",
      "product_description": "Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile;  and Medical Action Industries Inc. IV Start Kit, REF #78019 (on kit label), sterile.  Kit components are the Port Access Kit.",
      "code_info": "Port Access Kit case label - Lot 294281, exp. 9/28/2023, UDI #1080916018095.\nIV Start Kit label - Lot 294589, exp. 12/20/2024, UDI #20809160195991.",
      "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 Port Access Kits were incorrectly labeled as IV Start Kits on the kit label.  The case label was correctly labeled as Port Access Kits.",
      "root_cause_description": "Employee error",
      "action": "The recalling firm issued a letter dated 10/12/2022 to their only consignee via email on 10/12/2022.  The letter informed the consignee the kits were incorrectly labeled as reference number 78019, the IV Start Kit, but the case label correctly lists the item as the Port Access Kit.  The consignee was requested to review their inventory and segregate and quarantine all affected kits labeled as IV Start Kit, lot #294589.  If any of the affected kits were further distributed, the consignee was requested to ensure all end users were appropriately notified of the recall.  The consignee was to contact the firm for return of the affected kits.  A Field Action Response Form was enclosed for completion and return to the firm via email to indicate they have read and understood the recall instructions, checked their inventory, indicated how much was in inventory, and have notified appropriate staff and customers of the recall.",
      "product_quantity": "24 cases (480 kits)",
      "distribution_pattern": "Distribution was made to MN.  There was no foreign/government/military distribution.",
      "openfda": {
        "registration_number": [
          "2245270",
          "3012536737",
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        "fei_number": [
          "2245270",
          "1000512168",
          "3012536737",
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        ],
        "device_name": "Peripheral Catheter Insertion Kit",
        "medical_specialty_description": "General Hospital",
        "regulation_number": "880.5200",
        "device_class": "2"
      }
    }
  ]
}