{
  "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": "2026-07-08",
    "results": {
      "skip": 0,
      "limit": 1,
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    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Highland",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "89334",
      "recalling_firm": "ULTRAtab Laboratories, Inc.",
      "address_1": "50 Toc Dr",
      "address_2": "N/A",
      "postal_code": "12528-1506",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Bulk product was distributed to 3 distributors who may have distributed finished product.",
      "recall_number": "D-0526-2022",
      "product_description": "Kramer Novis Tusicof Caplet (Guaifenesin 400 mg, Dextromethorphan HBr 20 mg, Phenylephrine HCl 10 mg) Bulk Container, ULTRAtab Laboratories, Inc., Highland, NY  NDC 62959-124-00",
      "product_quantity": "639,729 tablets",
      "reason_for_recall": "CGMP Deviations",
      "recall_initiation_date": "20220126",
      "center_classification_date": "20220209",
      "termination_date": "20250107",
      "report_date": "20220216",
      "code_info": "Product Codes: C119L  Bulk Lots: 18K028"
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}