{
  "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": "2026-03-18",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "South Beloit",
      "state": "IL",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "78359",
      "recalling_firm": "Precision Dose Inc.",
      "address_1": "722 Progressive Ln",
      "address_2": "N/A",
      "postal_code": "61080-2616",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0057-2018",
      "product_description": "Carbamazepine Oral Suspension USP, 100 mg/5 mL, 5 mL Unit Dose Cups (NDC 68094-301-59), packaged in 10-count cups per tray, 3 trays per case containing a total of 5 mL x 30 Unit Dose Cups per case (NDC 68094-301-62), Rx only, Pkg: Precision Dose, Inc., S. Beloit, IL  61080.",
      "product_quantity": "801 cases",
      "reason_for_recall": "Subpotent Drug: low out of specification results.",
      "recall_initiation_date": "20170925",
      "center_classification_date": "20171101",
      "termination_date": "20180423",
      "report_date": "20171108",
      "code_info": "Lot number: 500105, Exp 04/30/18"
    }
  ]
}