{
  "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": {
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      "status": "Terminated",
      "city": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "91180",
      "recalling_firm": "Medical Action Industries, Inc. 306",
      "address_1": "25 Heywood Rd",
      "address_2": "",
      "postal_code": "28704-9302",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "US Nationwide distribution in the state of VA.",
      "recall_number": "Z-0751-2023",
      "product_description": "Medical Action INDUSTRIES INC. Port a Cath Kit REF 58647D, cardiac catheter introduction kit",
      "product_quantity": "198 cases",
      "reason_for_recall": "XXX",
      "recall_initiation_date": "20221104",
      "center_classification_date": "20221221",
      "termination_date": "20260318",
      "report_date": "20221228",
      "code_info": "UDI/DI 10809160156681, Lot Numbers:  297223, 297418",
      "more_code_info": ""
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}