{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Lutz",
      "address_1": "15402 N Nebraska Ave Ste 204",
      "reason_for_recall": "Recalled products do not have FDA approval for sale in the United States.",
      "address_2": "",
      "product_quantity": "1,781 cases",
      "code_info": "All lot numbers under item codes ending in -01: 4251601-01, 4251628-01, 4251652-01, 4251687-01, 4251890-01, 4252500-01, 4252519-01, 4252527-01, 4252535-01, 4252543-01, 4252560-01, 4252586-01, 4252594-01, 4253523-01, 4253540-01, 4254546-01.",
      "center_classification_date": "20210127",
      "distribution_pattern": "US Nationwide distribution including in the states of AL, CA, CT, FL, GA, IL, KS, LA, MI, MN, NC, NJ, NY, PA, SD, TX, WA.",
      "state": "FL",
      "product_description": "B. Braun Introcan IV Safety Catheters, sterile - Product Usage: It is a single-use device to generate intravascular and tissue access to sample blood, monitor blood pressure, or administer fluids and blood intravascular.",
      "report_date": "20210203",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Braxton Medical Corporation",
      "recall_number": "Z-0930-2021",
      "initial_firm_notification": "Letter",
      "product_type": "Devices",
      "event_id": "86443",
      "more_code_info": "",
      "recall_initiation_date": "20200904",
      "postal_code": "33549-6149",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Ongoing"
    }
  ]
}