{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
      "limit": 1,
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  "results": [
    {
      "country": "United States",
      "city": "Earth City",
      "address_1": "13480 Lakefront Dr",
      "reason_for_recall": "Labeling: Label Error on Declared Strength-The recalled product has a misprint on the Amoldipine 10 mg label, 5 mg is listed in the USP description.  Tablet strength is 10 mg.",
      "address_2": "",
      "product_quantity": "484,236 cartons",
      "code_info": "Lot # 130251, 130252, 130253 Exp date: 11/14",
      "center_classification_date": "20130516",
      "distribution_pattern": "Nationwide",
      "state": "MO",
      "product_description": "Walmart Amlodipine Besylate Tablets, USP 10 mg, Rx only, 30 tablets, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge, NY. Manufactured for: Camber Pharmaceuticals, Inc., Piscataway, NJ. Distributed by: Wal-Mart Stores, Inc., Bentonville, AR.  Packaged by: Legacy Pharmaceutical Packaging, LLC, Earth City, MO. NDC 68645-445-70.",
      "report_date": "20130522",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Legacy Pharmaceutical Packaging LLC",
      "recall_number": "D-319-2013",
      "initial_firm_notification": "Telephone",
      "product_type": "Drugs",
      "event_id": "64974",
      "termination_date": "20140213",
      "more_code_info": "",
      "recall_initiation_date": "20130422",
      "postal_code": "63045-1516",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}