{
  "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,
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  "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-0650-2018",
      "product_description": "Multi Lumen Central Venous Catheterization Kit; Product Code: ASK-12703-HH2;  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 number: 23F17C0652"
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}