{
  "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": "ASK-45552-RWJ4  13F16J0286  13F16L0014  13F17A0217  13F17D0222  13F17E0849  13F17F0784  13F17G0413",
      "center_classification_date": "20180313",
      "distribution_pattern": "US in the states of OH, FL, SC, TX, KY, NJ, MI",
      "state": "PA",
      "product_description": "Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R) PICC  Kit with Chlorag+ard(R) Technology    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: \u001c multiple infusions of fluids, medications, or chemotherapy \u001c infusion of fluids that are hypertonic, hyperosmolar, or have \u001c divergent pH values \u001c frequent blood sampling or blood/blood component infusions \u001c infusion of incompatible medications \u001c central venous pressure monitoring \u001c lack of usable peripheral IV sites \u001c replacement of multiple peripheral sites for IV access \u001c injection of contrast media \u001c 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-0996-2018",
      "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"
    }
  ]
}