{
  "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": {
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    {
      "status": "Terminated",
      "city": "Princeton",
      "state": "NJ",
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      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
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      "recalling_firm": "Dr. Reddy's Laboratories, Inc.",
      "address_1": "107 College Rd E",
      "address_2": "N/A",
      "postal_code": "08540-6623",
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      "product_description": "Allergy Relief D Fexofenadine HCl, 60 mg I Pseudoephedrine HCl, 120 mg, Extended Release Tablets, USP,  30 Extended-Release Tablets USP,  Distributed By Walmart Inc., Bentonville, AR  72716, Product of India, NDC 49035-273-30.",
      "product_quantity": "9,984 cartons",
      "reason_for_recall": "Failed dissolution specifications",
      "recall_initiation_date": "20211112",
      "center_classification_date": "20211207",
      "termination_date": "20230623",
      "report_date": "20211215",
      "code_info": "Lot #: AC2103329B",
      "more_code_info": ""
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}