{
  "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": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "93074",
      "recalling_firm": "B. Braun Medical, Inc.",
      "address_1": "901 Marcon Blvd",
      "address_2": "",
      "postal_code": "18109-9512",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Worldwide distribution - US Nationwide and the countries of Canada and Singapore.",
      "recall_number": "Z-0130-2024",
      "product_description": "AMO ADMINISTRATION SET, Article No. 7A3817, REF OM2505191, for ophthalmologic use.",
      "product_quantity": "32,000",
      "reason_for_recall": "Devices may leak as a result of a manufacturing issue. Leakage may result in a delay of therapy, increase risk of bloodstream infection (BSI), and may expose both patients and healthcare workers to hazardous medication.  There is also the potential for life-threatening situations to occur requiring additional medical intervention.",
      "recall_initiation_date": "20230926",
      "center_classification_date": "20231103",
      "report_date": "20231115",
      "code_info": "UDI-DI: 4046964183454  Lots 0061747706 0061752064 0061755195 0061790409",
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