{
  "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": "2026-04-08",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "83478",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Blvd",
      "address_2": "N/A",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "CA  FL  MO  TX  MN  AL  GA  NC  IL  PA",
      "recall_number": "Z-2471-2019",
      "product_description": "CE17TKFCSN  CON EPI TRAY W/17G TUHY NRFIT  Catalog # 339187",
      "product_quantity": "200 units",
      "reason_for_recall": "The filter capacity is not achieved due to damage of the filter membrane.",
      "recall_initiation_date": "20190710",
      "center_classification_date": "20190905",
      "termination_date": "20200821",
      "report_date": "20190911",
      "code_info": "Lot # 0061620275    UDI: 04046964941412"
    }
  ]
}