{
  "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": "2026-06-03",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Lake Zurich",
      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
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        "route": [
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          "17271-701-03",
          "17271-701-05",
          "17271-701-06",
          "17271-701-07"
        ],
        "is_original_packager": [
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        "unii": [
          "451W47IQ8X"
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      },
      "product_type": "Drugs",
      "event_id": "98581",
      "recalling_firm": "Fresenius Kabi USA, LLC",
      "address_1": "3 Corporate Dr",
      "address_2": "",
      "postal_code": "60047-8930",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "US Nationwide , Alaska, and Puerto Rico.",
      "recall_number": "D-0434-2026",
      "product_description": "0.9% Sodium Chloride Injection, USP 900 mg per 100 mL (9 mg per mL), 1,000 mL in a Single Dose freeflex bag, Rx only, BD Becton, Dickson and Company, 1 Becton Drive, Franklin Lakes, NJ 07417, Distributed by BD, Manufactured by Fresenius Kabi, Unit of Sale NDC Number: 17271-701-07.",
      "product_quantity": "",
      "reason_for_recall": "Lack of Assurance of Sterility",
      "recall_initiation_date": "20260311",
      "center_classification_date": "20260403",
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      "code_info": "Batch# 24EU10010, Exp Date: 05/31/2027.",
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}