{
  "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
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  },
  "results": [
    {
      "country": "United States",
      "city": "Glasgow",
      "address_1": "118 Beaver Trl",
      "reason_for_recall": "Failed Dissolution Specifications",
      "address_2": "",
      "product_quantity": "105,215 Bottles",
      "code_info": "Lot #: a) AR151324, AR151322, AR151325,  Exp. 9/2017; AR160730A, AR160731A, AR160732A, Exp. 05/2018.  b) AR151324, AR151322, AR151325, Exp. 9/2017; AR160730B, 5/2018.",
      "center_classification_date": "20170502",
      "distribution_pattern": "Nationwide within the US and PR",
      "state": "KY",
      "product_description": "Rabeprazole Sodium Delayed Release Tablets, 20 mg, a) 30-count bottle (NDC 65162-0724-03), b) 90-count bottle (NDC 65162-0724-09), Rx Only, Manufactured by Amneal Pharmaceuticals Pvt. Ltd., Ahmedabad INDIA 382220, Distributed by Amneal Pharmaceuticals, Bridgewater, NJ 08807",
      "report_date": "20170510",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Amneal Pharmaceuticals LLC",
      "recall_number": "D-0693-2017",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "76627",
      "termination_date": "20190411",
      "more_code_info": "",
      "recall_initiation_date": "20161212",
      "postal_code": "42141-1273",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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  ]
}