{
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    "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": "2026-07-29",
    "results": {
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      "status": "Terminated",
      "city": "Ronkonkoma",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "88322",
      "recalling_firm": "Spirit Pharmaceuticals",
      "address_1": "2004 Orville Dr N Ste 2",
      "address_2": "N/A",
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      "product_description": "Acetaminophen 325 mg tablets, Regular Strength Pain Reliever, 100-count bottle, Distributed by: Walmart Inc., Bentoville, AR 72716, NDC 79903-052-10",
      "product_quantity": "N/A",
      "reason_for_recall": "cGMP deviations: Discolored acetaminophen",
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      "center_classification_date": "20210816",
      "termination_date": "20220907",
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      "code_info": "Lot #: S210240, Exp. 03/2023"
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