{
  "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,
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      "state": "IL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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        "unii": [
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      },
      "product_type": "Drugs",
      "event_id": "97453",
      "recalling_firm": "Baxter Healthcare Corporation",
      "address_1": "1 Baxter Pkwy",
      "address_2": "",
      "postal_code": "60015-4625",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S.A. Nationwide",
      "recall_number": "D-0596-2025",
      "product_description": "Acetaminophen Injection 1000 mg/100 mL (10 mg/mL), packaged in 100 mL Viaflo container, Rx only, Baxter Healthcare Corporation, Deerfield, IL 60015, Made in Ireland, NDC 36000-306-60.",
      "product_quantity": "13,000 containers",
      "reason_for_recall": "Discoloration",
      "recall_initiation_date": "20250820",
      "center_classification_date": "20250822",
      "report_date": "20250903",
      "code_info": "Lot #: 24A27G66, Exp 12/31/2025",
      "more_code_info": ""
    }
  ]
}