{
  "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,
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    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "East Brunswick",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {
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          "ANDA212329"
        ],
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        "substance_name": [
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        "is_original_packager": [
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      "product_type": "Drugs",
      "event_id": "98321",
      "recalling_firm": "Unichem Pharmaceuticals USA Inc.",
      "address_1": "1 Tower Center Blvd Ste 2200",
      "address_2": "N/A",
      "postal_code": "08816-1145",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-0306-2026",
      "product_description": "Doxazosin Tablets, USP, 4 mg, 1000 tablets per bottle, Rx only, distributed by Unichem Pharmaceuticals (USA), Inc., 1 Tower Center Boulevard, Suite 2200, East Brunswick, NJ 08816 USA, manufactured by Unichem Laboratories Limited, Plot Number 15 to 18, Pilerne Industrial Estate, Pilerne, Bardez, Goa (India) 403511, NDC 29300-353-10.",
      "product_quantity": "60,000 tablets",
      "reason_for_recall": "Tablets/Capsules Imprinted with Wrong ID",
      "recall_initiation_date": "20260121",
      "center_classification_date": "20260211",
      "report_date": "20260218",
      "code_info": "Lot # GDSH25006, Exp Date: 08/2027"
    }
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}