{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "79197",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Rd",
      "address_2": "N/A",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Distribution US Nationwide",
      "recall_number": "Z-0658-2018",
      "product_description": "ARROWg+ard Blue Two Lumen Hemodialysis Catheterization Kit for High Volume Infusions; Product Codes: AK-22142-CDC, AK-22142-F, AK-25142-CDC, AK-25142-F; Exp. Dates Feb 2018 - Nov 2018",
      "product_quantity": "5,926 total",
      "reason_for_recall": "These finished good kits may contain the incorrect Springwire Guide (SWG).",
      "recall_initiation_date": "20171017",
      "center_classification_date": "20180220",
      "termination_date": "20200414",
      "report_date": "20180228",
      "code_info": "Lot numbers:  Product Code AK-22142-CDC:  13F17A0021  13F17A0315    Product Code AK-22142-F:  13F17B0338  13F17E0067    Product Code AK-25142-CDC:  13F17E0340    Product Code AK-25142-F:  13F17A0207"
    }
  ]
}