{
  "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": "2026-07-29",
    "results": {
      "skip": 0,
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    }
  },
  "results": [
    {
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      "city": "Piscataway",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
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          "31722-713-32",
          "31722-713-31",
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        ],
        "is_original_packager": [
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          "0331722713900",
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        ]
      },
      "product_type": "Drugs",
      "event_id": "91855",
      "recalling_firm": "Hetero USA Inc",
      "address_1": "1035 Centennial Ave",
      "address_2": "N/A",
      "postal_code": "08854-4124",
      "voluntary_mandated": "N/A",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide within the United States",
      "recall_number": "D-0530-2023",
      "product_description": "Pantoprazole Sodium Delayed Release Tablets USP 40mg, 1000-count bottles, Rx only, Manufactured for: Camber Pharmaceuticals Inc., Piscataway, NJ, 08854, By: Hetero Labs Limited, Unit V, Polepally, Jadcherla, Mahabubnagar- 509 301, India NDC 31722-713-10",
      "product_quantity": "2,352 bottles",
      "reason_for_recall": "CGMP Deviations: Discoloration",
      "recall_initiation_date": "20230314",
      "center_classification_date": "20230411",
      "report_date": "20230419",
      "code_info": "Lot #: PAN22542, Exp. Date: 9/2024"
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}