{
  "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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      "city": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
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      "postal_code": "07054-1120",
      "voluntary_mandated": "Voluntary: Firm initiated",
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      "distribution_pattern": "Nationwide",
      "recall_number": "D-0275-2024",
      "product_description": "Budesonide Extended-Release Tablets 9mg, 30-count bottle, Rx Only,  Manufactured by: Actavis Laboratories FL, Inc., Fort Lauderdale, FL 33314 USA, Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054 USA, NDC 0591-2510-30",
      "product_quantity": "10,672 30-count bottles",
      "reason_for_recall": "Failed Dissolution Specifications",
      "recall_initiation_date": "20240108",
      "center_classification_date": "20240126",
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      "code_info": "Lot # 100047273; Exp. 07/2025",
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}