{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "country": "United States",
      "city": "Richland",
      "address_1": "199 Interstate Dr Ste N",
      "reason_for_recall": "CGMP Deviations; deficiencies at the manufacturer  may result in assay or content uniformity failures",
      "address_2": "",
      "product_quantity": "11,539 bottles",
      "code_info": "(a) LOT # 28981501, EXP 8/17, NDC 35573-302-30;    (b) LOT # 28981501, EXP 8/17, LOT # 28981601, EXP 4/18, NDC 35573-302-10",
      "center_classification_date": "20161129",
      "distribution_pattern": "Nationwide",
      "state": "MS",
      "product_description": "UROLET MB URINARY ANTISEPTIC, ANTISPASMODIC Tablets, Each tablet contains:  Methenamine 81.6 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue, 10.8 mg; Hyoscyamine Sulfate, 0.12 mg, (a) 30 count (NDC 35573-302-30) and (b) 100 count bottles (NDC 35573-302-10), Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS",
      "report_date": "20161207",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Burel Pharmaceuticals Inc",
      "recall_number": "D-0156-2017",
      "initial_firm_notification": "E-Mail",
      "product_type": "Drugs",
      "event_id": "75566",
      "termination_date": "20170814",
      "more_code_info": "",
      "recall_initiation_date": "20161024",
      "postal_code": "39218-9433",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}