{
  "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": {
      "skip": 0,
      "limit": 1,
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    }
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  "results": [
    {
      "status": "Ongoing",
      "city": "Pulaski",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
        "application_number": [
          "ANDA091232"
        ],
        "brand_name": [
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        ],
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        "product_type": [
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        ],
        "rxcui": [
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          "748797",
          "749155",
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          "749157"
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          "42291-565-84"
        ],
        "is_original_packager": [
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        ]
      },
      "product_type": "Drugs",
      "event_id": "97542",
      "recalling_firm": "AvKARE",
      "address_1": "615 N 1st St",
      "address_2": "",
      "postal_code": "38478-2403",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "U.S. Nationwide",
      "recall_number": "D-0007-2026",
      "product_description": "Norgestimate and Ethinyl Estradiol Tablets, USP, 0.18 mg/0.025 mg, 0.215 mg/0.025 mg, and 0.25 mg/0.025 mg, 3 Units, 3x28 tablets blister cards per carton, Rx only,  Manufactured for AvKARE, Pulaski, TN 38478.  Carton NDC:  42291-565-84; Blister NDC:  42291-565-28",
      "product_quantity": "2192 cartons",
      "reason_for_recall": "Failed Content Uniformity Specifications",
      "recall_initiation_date": "20250902",
      "center_classification_date": "20251006",
      "report_date": "20251015",
      "code_info": "Lot # LF41138A; Exp 06/30/2027",
      "more_code_info": ""
    }
  ]
}