{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Eysins",
      "state": "",
      "country": "Switzerland",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "96399",
      "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": "U.S.: AK, AL, AR, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NM, NV, OH, OK, OR, PA, SC, TN. TX, UT, VA, WA, WV  O.U.S.: N/A",
      "recall_number": "Z-1509-2025",
      "product_description": "BD Connecta BD Luer-Lok 360, REF 394910  UDI-DI code: 00382903949106    Connecta¿ Plus 1 and Connecta¿ Plus 3 2-way and 3-way Stopcocks are control valves for use in IV. therapy and hemodynamic pressure monitoring.",
      "product_quantity": "500 units",
      "reason_for_recall": "Due to specific lots of luer-lok devices were shipped to the U.S. market with an Outside US Instruction for Use (IFU)",
      "recall_initiation_date": "20250220",
      "center_classification_date": "20250402",
      "report_date": "20250409",
      "code_info": "Catalog Number: 394910 UDI-DI code: 00382903949106 Lot Numbers: 4277968 4277973 4282451 4282461 4289801 4290582 4292904 4295848 4305108 4306700",
      "more_code_info": ""
    }
  ]
}