{
  "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,
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  "results": [
    {
      "country": "United States",
      "city": "Parsippany",
      "address_1": "20 Waterview Blvd., Suite 3",
      "reason_for_recall": "Failed Dissolution Specifications; 12 month acid dissolution test results were above upper limit specifications.",
      "address_2": "",
      "product_quantity": "1129 bottles",
      "code_info": "Lot: #: DM12286, Expiry: 06/14.",
      "center_classification_date": "20140129",
      "distribution_pattern": "Nationwide including Puerto Rico",
      "state": "NJ",
      "product_description": "Pantaprazole Sodium Delayed Release Tablets , USP 40 mg, 1000 tablets bottle, Rx only. Manufactured by: Wockhardt Limited, Mumbai, India.  Distributed by: Wockhardt USA LLC 20 Waterview Blvd Parsippany, NJ 07054 USA.  NDC: 64679-0434-02.",
      "report_date": "20140205",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Wockhardt Usa Inc.",
      "recall_number": "D-1042-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "67238",
      "termination_date": "20150129",
      "more_code_info": "",
      "recall_initiation_date": "20131127",
      "postal_code": "07054",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}