{
  "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": "2026-07-22",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Allentown",
      "state": "PA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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        ],
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        ],
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        ],
        "product_type": [
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        "route": [
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        "substance_name": [
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          "0264-7800-20",
          "0264-7802-00",
          "0264-7802-10"
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        "is_original_packager": [
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "97368",
      "recalling_firm": "B BRAUN MEDICAL INC",
      "address_1": "861 Marcon Blvd",
      "address_2": "N/A",
      "postal_code": "18109-9577",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the US",
      "recall_number": "D-0586-2025",
      "product_description": "0.9% Sodium Chloride Injection USP, L 8000, 1000mL Excel Container, Rx Only, Sterile, nonpyrogenic, single dose container, B. Braun Medical Inc., Bethlehem, PA 18018, NDC 0264-7800-00.",
      "product_quantity": "23,100 containers",
      "reason_for_recall": "Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.",
      "recall_initiation_date": "20250804",
      "center_classification_date": "20250814",
      "report_date": "20250820",
      "code_info": "Lot #: J5C919, Exp. 08/31/2027",
      "more_code_info": ""
    }
  ]
}