{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Breinigsville",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "90830",
      "recalling_firm": "B Braun Medical Inc",
      "address_1": "200 Boulder Dr",
      "address_2": "N/A",
      "postal_code": "18031-1532",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Domestic distribution to AZ CA FL GA MD MI MO MS NC NY OH PA TN TX WA.  Foreign distribution to Canada",
      "recall_number": "Z-0009-2023",
      "product_description": "Introcan Safety FEP 14G, 2.2x32MM-US, Product Code 4251890-02.  A passive anti-needle device to provide venous or arterial access.",
      "product_quantity": "94,000 US",
      "reason_for_recall": "Potential for leakage at the catheter hub.",
      "recall_initiation_date": "20220901",
      "center_classification_date": "20221006",
      "report_date": "20221012",
      "code_info": "UDI-DI (GTIN): 04046963318154  Lot Number/Expiration Date: 22D04G8241 01 Apr 2027 22D07G8241 01 Apr 2027 22D07G8242 01 Apr 2027 22E30G8241 01 May 2027 22E30G8242 01 May 2027"
    }
  ]
}