{
  "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": "2026-04-15",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Some of the products listed in the recall may be missing a sticker that contains the lot number, expiration date, and Unique Device Identification (UDI) information.",
      "address_2": "",
      "product_quantity": "23,904 in total",
      "code_info": "CDA-45854-P1A  13F17C0325  13F17D0283  13F17F0748",
      "center_classification_date": "20180313",
      "distribution_pattern": "US in the states of OH, FL, SC, TX, KY, NJ, MI",
      "state": "PA",
      "product_description": "ARROWg+ard BLUE PLUS  Pressure Injectable Quad- Lumen CVC Kit    Product Usage:  The Arrow¿ CVC is indicated to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to:   multiple infusions of fluids, medications, or chemotherapy   infusion of fluids that are hypertonic, hyperosmolar, or have   divergent pH values   frequent blood sampling or blood/blood component infusions   infusion of incompatible medications   central venous pressure monitoring   lack of usable peripheral IV sites   replacement of multiple peripheral sites for IV access   injection of contrast media   When used for pressure injection of contrast media, do not exceed the maximum indicated flow rate for each catheter lumen. The maximum pressure of power injector equipment used with pressure injectable CVC may not exceed 400 PSI.",
      "report_date": "20180321",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-1005-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "79339",
      "termination_date": "20200922",
      "more_code_info": "",
      "recall_initiation_date": "20171127",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}