{
  "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": "2026-04-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Lot Number: 13F17F0081",
      "center_classification_date": "20180410",
      "distribution_pattern": "Distributed in all 50 U.S. states and the District of Columbia. Distributed in Bahamas, Canada, Mexico, Panama, and Singapore.",
      "state": "PA",
      "product_description": "Multi-Lumen Hemodialysis Catheterization Kit for High Volume Infusions, Part Number: CDC-12123-P1A",
      "report_date": "20180418",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-1328-2018",
      "initial_firm_notification": "E-Mail",
      "product_type": "Devices",
      "event_id": "79512",
      "termination_date": "20200527",
      "more_code_info": "",
      "recall_initiation_date": "20171222",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}