{
  "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": "2026-09-16",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Deerfield",
      "state": "IL",
      "country": "United States",
      "classification": "Class I",
      "openfda": {
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        ],
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        "is_original_packager": [
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      "product_type": "Drugs",
      "event_id": "99678",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "N/A",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Natonwide in the USA",
      "recall_number": "D-0849-2026",
      "product_description": "0.9% Sodium Chloride Injection USP 500 mL, VIAFLEX Plastic Containers, with 24 units per case. Baxter Healthcare Corporation, Deerfield, IL, 60015, USA, Made in USA, NDC 0338-0049-03",
      "product_quantity": "145,464 500mL bags",
      "reason_for_recall": "Presence of particulate matter: Particulates identified as fiberglass",
      "recall_initiation_date": "20260817",
      "center_classification_date": "20260915",
      "report_date": "20260909",
      "code_info": "Lot: Y495523, Y495523A, Exp 31-Oct-2027",
      "more_code_info": ""
    }
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}