{
  "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": "Bridgewater",
      "address_1": "400 Somerset Corporate Blvd",
      "reason_for_recall": "Labeling: Incorrect or Missing Package Insert: Package insert is missing warning regarding anaphylaxis.",
      "address_2": "",
      "product_quantity": "958 Bottles",
      "code_info": "Lot #: 2555979, Expiry: 09/2016.",
      "center_classification_date": "20160630",
      "distribution_pattern": "US Nationwide",
      "state": "NJ",
      "product_description": "SECONAL SODIUM (secobarbital sodium) Capsules, USP, 100 mg, 100 Ct. Bottles, Rx Only. Distributed by: Valeant Pharmaceuticals North America, LLC, Bridgewater, NJ 08807. NDC: 0187-4220-10.",
      "report_date": "20160706",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Valeant Pharmaceuticals North America LLC",
      "recall_number": "D-1059-2016",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "74532",
      "termination_date": "20170614",
      "more_code_info": "",
      "recall_initiation_date": "20160610",
      "postal_code": "08807-2867",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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}