{
  "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": "2026-03-18",
    "results": {
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      "city": "Houston",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
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      "recalling_firm": "Pharm D Solutions, LLC",
      "address_1": "1304 S Loop W",
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      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Press Release",
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      "recall_number": "D-0138-2019",
      "product_description": "Ascorbic Acid 500 mg/mL Solution Pharm D Solutions, Houston, Texas --- NDC 69699-1502-50",
      "product_quantity": "10000 milliliters",
      "reason_for_recall": "Lack of Assurance of Sterility",
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      "center_classification_date": "20181101",
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      "code_info": "Lot: 04252018:91 Discard by: 10/21/2018"
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