{
  "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 II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "77732",
      "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": "Telephone",
      "distribution_pattern": "OH and CT",
      "recall_number": "D-1037-2017",
      "product_description": "Carbamazepine Oral Suspension, USP. 100 mg/5 mL, 5 mL Unit Dose Cups, Rx Only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080, NDC 68094-301-59.",
      "product_quantity": "480 (5mL) unit dose cups",
      "reason_for_recall": "Labeling Error: Label mix-up.  Products' unit dose cups are correctly labeled, but the product carton lists incorrect volume and NDC.",
      "recall_initiation_date": "20170705",
      "center_classification_date": "20170731",
      "termination_date": "20180328",
      "report_date": "20170809",
      "code_info": "Lot #: 500326, Exp. 6/30/2018"
    }
  ]
}