{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Eysins",
      "state": "N/A",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "94479",
      "recalling_firm": "BD SWITZERLAND SARL",
      "address_1": "Terre Bonne Park A4",
      "address_2": "Route De Crassier 17",
      "postal_code": "N/A",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide - US Nationwide distribution in the states of AR, CA, CO, IL, KS, MA, ME, NJ, NY, PA, SD, WA and WI. The country of Canada.",
      "recall_number": "Z-1944-2024",
      "product_description": "Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Check Valve 2 SmartSite Y Sites  REF 10013072  Tubing set used for delivery of fluids, medication, blood and blood products.",
      "product_quantity": "11.300 sets",
      "reason_for_recall": "Due to infusion set tubing drip chamber becoming detached from the tubing potentially causing delays in treatment, or unintentionally exposing users to harsh infusates.",
      "recall_initiation_date": "20240418",
      "center_classification_date": "20240531",
      "report_date": "20240612",
      "code_info": "Catalog Number: 10013072 UDI-DI code:07613203021210 Lot Number:  22115368",
      "more_code_info": ""
    }
  ]
}