{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Reading",
      "address_1": "2400 Bernville Rd",
      "reason_for_recall": "Products may contain the incorrect banner card within the kit",
      "address_2": "",
      "product_quantity": "231 units",
      "code_info": "Lot Number: 13F18H0499",
      "center_classification_date": "20190923",
      "distribution_pattern": "US Nationwide distribution.",
      "state": "PA",
      "product_description": "Arrow 8.5 Fr. X 16 cm Quad-Lumen Central Venous Catheterization Kit  Product Code:AK-42854-P1A - Product Usage: The Arrow Central Venous Catheters are intended to permit venous access to the central circulation by way of the femoral, jugular or subclavian veins.",
      "report_date": "20191002",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2556-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "83593",
      "termination_date": "20200929",
      "more_code_info": "",
      "recall_initiation_date": "20190806",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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  ]
}