{
  "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": "The recalling firm has received complaints related to increased resistance encountered when introducing the CVC over the spring wire guide. This may lead to procedural delay, and there may be need of medical intervention by exchanging the catheter for another CVC catheter.",
      "address_2": "",
      "product_quantity": "1200",
      "code_info": "71F18A0682",
      "center_classification_date": "20180629",
      "distribution_pattern": "Distributor in FL. International distribution to Czech Republic, Dominican Republic, France, Greece, and Italy.",
      "state": "PA",
      "product_description": "Multi-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter, CS-15853-E    Product CVCs are intended to permit venous access to the central circulation through a single puncture site by way of the femoral, jugular, or subclavian veins.",
      "report_date": "20180711",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Arrow International Inc",
      "recall_number": "Z-2336-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "80227",
      "termination_date": "20200420",
      "more_code_info": "",
      "recall_initiation_date": "20180511",
      "postal_code": "19605-9607",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}