{
  "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": "Pine Brook",
      "address_1": "10 Bloomfield Ave",
      "reason_for_recall": "Failed Content Uniformity Specifications - The lot failed to meet the acceptance criteria for Uniformity of Dosage Units at the time of release for the oxycodone component.",
      "address_2": "Building B, Suite 2",
      "product_quantity": "8,964 (100 Count) bottles",
      "code_info": "NDC #47781-0230-01; Lot # 453289; Exp 08/31/15",
      "center_classification_date": "20140923",
      "distribution_pattern": "Nationwide",
      "state": "NJ",
      "product_description": "Oxycodone and Acetaminophen Tablets USP 10 mg/325 mg 100 count bottles Rx Only.  Manufactured by Norwich Pharmaceuticals Inc., Norwich, NY  13185 USA; Distributed by Alvogen Inc, Pine Brook NJ 07058 USA.",
      "report_date": "20141001",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Alvogen, Inc",
      "recall_number": "D-1607-2014",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "69159",
      "termination_date": "20150430",
      "recall_initiation_date": "20140828",
      "postal_code": "07058-9743",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}