{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Bristol",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "64405",
      "recalling_firm": "Dr Reddys Laboratories Tennessee LLC",
      "address_1": "201 Industrial Dr",
      "address_2": "N/A",
      "postal_code": "37620-5413",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-239-2013",
      "product_description": "Amoxicillin for Oral Suspension, 125mg/5mL,  a) 80 mL (NDC 43598-222-80); b) 100mL, (NDC 43598-222-52); c)150 mL (NDC 43598-222-53) bottles, Rx only, Dist. By:  Dr. REDDY'S Laboratories, Inc., Bridgewater, NJ  08807",
      "product_quantity": "4236 Bottles",
      "reason_for_recall": "Microbial Contamination of Non-Sterile Products: Suspensions made from these lots of Amoxicillin 125 mg/5 mL showed yeast and mold growth at the 14 day time point.",
      "recall_initiation_date": "20130215",
      "center_classification_date": "20130402",
      "termination_date": "20131001",
      "report_date": "20130410",
      "code_info": "Lot #s: a) T200112; b) T200103, T200113; c) T200104, T200114"
    }
  ]
}