{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77951",
      "recalling_firm": "Wockhardt Usa Inc.",
      "address_1": "20 Waterview Blvd Ste 3",
      "address_2": "N/A",
      "postal_code": "07054-1271",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0051-2018",
      "product_description": "Enalapril Maleate tablets, USP, 5mg, 1000-count bottles, Rx only, Manufactured by: Wockhardt Limited H-14/2, M.I.D.C. Area, Waluj, Aurangabad, Maharashtra, India, Distributed by: Wockhardt, USA LLC, 20 Waterview Blvd, Parsippany, NJ 07054, USA. NDC: 64679-924-03;",
      "product_quantity": "5050 bottles",
      "reason_for_recall": "Failed Impurities/Degradation Specifications: 5mg strength being recalled for out of specification results for related compound.",
      "recall_initiation_date": "20170822",
      "center_classification_date": "20171026",
      "termination_date": "20190227",
      "report_date": "20171101",
      "code_info": "Lot # DR10635, EXP 05/2019; DR10636, EXP 05/2019."
    }
  ]
}