{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91065",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "address_2": "N/A",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution was made to MN.  There was no foreign/government/military distribution.",
      "recall_number": "Z-0464-2023",
      "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.",
      "product_quantity": "24 cases (480 kits)",
      "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.",
      "recall_initiation_date": "20221012",
      "center_classification_date": "20221208",
      "termination_date": "20250325",
      "report_date": "20221214",
      "code_info": "Port Access Kit case label - Lot 294281, exp. 9/28/2023, UDI #1080916018095. IV Start Kit label - Lot 294589, exp. 12/20/2024, UDI #20809160195991."
    }
  ]
}