{
  "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": "Parsippany",
      "state": "NJ",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "67933",
      "recalling_firm": "Wockhardt Usa Inc.",
      "address_1": "20 Waterview Blvd., Suite 3",
      "address_2": "N/A",
      "postal_code": "07054",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide",
      "recall_number": "D-1300-2014",
      "product_description": "Metoprolol Succinate Extended-Release Tablets, USP, 50 mg, 30-count bottle, Rx only, Manufactured by: Wockhardt Limited, Mumbai, India; Distributed by: Wockhardt USA LLC., 20 Waterview Blvd., Parsippany, NJ  07054, USA; NDC 64679-735-09, UPC 3 64679 73509 1.",
      "product_quantity": "109,744 bottles",
      "reason_for_recall": "Failed Dissolution Specifications: failure of dissolution test observed at nine month time point.",
      "recall_initiation_date": "20140401",
      "center_classification_date": "20140502",
      "termination_date": "20150512",
      "report_date": "20140514",
      "code_info": "Lot #: LN10686, LN10687, LN10688, LN10707, LN10708, Exp 02/15"
    }
  ]
}