{
  "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": {
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  "results": [
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      "city": "Largo",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        "route": [
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        "pharm_class_epc": [
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        "pharm_class_cs": [
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      "product_type": "Drugs",
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      "recalling_firm": "VistaPharm LLC",
      "address_1": "7265 Ulmerton Rd",
      "address_2": "",
      "postal_code": "33771-4809",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "Distributed nationwide to 68 consignees in the U.S.",
      "recall_number": "D-1149-2023",
      "product_description": "Sucralfate Oral Suspension 1g per 10mL, FOR ORAL ADMINISTRATION ONLY (414 mL bottle), Rx Only, Manufactured and Distributed by: VistaPharm, Inc. Largo, FL 33771, NDC 66689-305-16",
      "product_quantity": "14,400 bottles",
      "reason_for_recall": "Superpotent/Subpotent single ingredient Drug: Out of Specification Assay results",
      "recall_initiation_date": "20230830",
      "center_classification_date": "20230911",
      "termination_date": "20240726",
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      "code_info": "Lot #: 921100; Exp. 02/2025",
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}