{
  "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": "2026-06-24",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Arden",
      "state": "NC",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "98698",
      "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": "Letter",
      "distribution_pattern": "US distribution to state of: AZ OUS: None",
      "recall_number": "Z-2007-2026",
      "product_description": "Medical Action Industries Inc.   Pack Cath BHH,   REF: BHCA49K, Sterile EO, Rx Only, QTY: 5/Case",
      "product_quantity": "2030 kits",
      "reason_for_recall": "Convenience kit contains a syringe in which the rotating adapter may unwind during use, resulting in a loose connection and/or full disconnection between the syringe and manifold\"",
      "recall_initiation_date": "20260317",
      "center_classification_date": "20260506",
      "report_date": "20260513",
      "code_info": "UDI:20809160490294/ Lot numbers: 342509, 346066, 338434, 339423, 337365, 335489, 336189, 336789",
      "more_code_info": ""
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}