{
  "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": "Chatsworth",
      "state": "CA",
      "country": "United States",
      "classification": "Class I",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "82758",
      "recalling_firm": "D.B.P. Distribution",
      "address_1": "23550 Ehlers Dr",
      "address_2": "",
      "postal_code": "91311-6310",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-1292-2019",
      "product_description": "Titanium 4000, capsule, 4000 mg, 1 count blister card, 30 blister display boxt, distributed by Titanium 4000  UPC 86077000020",
      "product_quantity": "unknown",
      "reason_for_recall": "Marketed without an approved NDA/ANDA: undeclared  sildenafil and tadalafil.",
      "recall_initiation_date": "20190423",
      "center_classification_date": "20190522",
      "termination_date": "20230307",
      "report_date": "20190522",
      "code_info": "Expiration 12/29/2020",
      "more_code_info": ""
    }
  ]
}