{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "La Vergne",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {
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        ],
        "brand_name": [
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        ],
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        "product_ndc": [
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        "product_type": [
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        ],
        "route": [
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        "rxcui": [
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        "package_ndc": [
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        "unii": [
          "660YQ98I10"
        ]
      },
      "product_type": "Drugs",
      "event_id": "96201",
      "recalling_firm": "The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories",
      "address_1": "341 Mason Rd",
      "address_2": "",
      "postal_code": "37086-3606",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0221-2025",
      "product_description": "Potassium Chloride Extended-Release Tablets, USP, 10 mEq (750 mg), 100 Tablets per carton (10 x 10 unit dose blisters), Rx Only, Distributed by: Aurobindo Pharma USA< INC., 279 Princeton-Hightstown Road, East Windsor, NJ 08520.  Made in India.  Distributed by: MAJOR PHARMACEUTICALS, Livonia, MI 48152.  NDC: 0904-7216-61",
      "product_quantity": "6997 cartons",
      "reason_for_recall": "Failed Dissolution Specifications.",
      "recall_initiation_date": "20250130",
      "center_classification_date": "20250204",
      "report_date": "20250212",
      "code_info": "Lot# T05224; Exp. 02/2026",
      "more_code_info": ""
    }
  ]
}