{
  "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,
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  "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-2472-2019",
      "product_description": "CE18TKN ACCU-BLOC PERIFIX KIT NRFIT  Catalog # 339188",
      "product_quantity": "3820 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 # 0061537846  Exp: 8/31/2018  Lot # 0061537847  Exp: 10/31/2018  Lot # 0061620282  Exp: 9/30/2019    UDI: 04046964941436"
    }
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}