{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Reading",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "69290",
      "recalling_firm": "Arrow International Inc",
      "address_1": "2400 Bernville Road",
      "address_2": "N/A",
      "postal_code": "19605",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Distribution including the states of MD, NC , LA , IN , OH, KY, CA , PA , NY and NV.",
      "recall_number": "Z-0076-2015",
      "product_description": "Multi-Lumen Central Venous Catheterization  Kit",
      "product_quantity": "65",
      "reason_for_recall": "Arrow International, Inc. has initiated a voluntary recall for product code AK-  12703, lot number RF3039028 because the label on the outer corrugate is labeled with the incorrect expiration date. All kits packaged within the corrugate are correctly labeled. There is no risk to the patient as the kits within the corrugate are labeled with the correct  expiration date.",
      "recall_initiation_date": "20140918",
      "center_classification_date": "20141016",
      "termination_date": "20141202",
      "report_date": "20141022",
      "code_info": "Catolog No - AK-12703  lot number RF3039028"
    }
  ]
}