{
  "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": "2026-04-01",
    "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": "81117",
      "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": "US nationwide in the states of CA, FL, NC, and RI.",
      "recall_number": "Z-0282-2019",
      "product_description": "Arrow AGB + Multi-Lumen CVC Kit, Cat. No. CDC-42703-B1A. Product Usage - The Arrow CVC is intended to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access, including, but not limited to the following: Lack of usable peripheral IV sites, Central venous pressure monitoring, Total parenteral nutrition (TPN), Infusions of fluids, medications, or chemotherapy, and Frequent blood sampling or receiving blood transfusions/blood products.",
      "product_quantity": "105",
      "reason_for_recall": "The product was  shipped after its expiry date due to a system error. The product lidstock identifies the  correct expiration date however the accompanying purchase order shipping  documentation identifies an incorrect expiration date. Per standard clinical practice the  lidstock would most likely be checked prior to use and the product would not be used  leading to a minor delay while a replacement is located. In the unlikely event that the  product lidstock is not checked prior to use, there is potential for use of expired  product, and product functionality/or sterility cannot be guaranteed.",
      "recall_initiation_date": "20180830",
      "center_classification_date": "20181026",
      "termination_date": "20200731",
      "report_date": "20181107",
      "code_info": "23F16C0071"
    }
  ]
}