{
  "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": [
    {
      "country": "United States",
      "city": "Edmond",
      "address_1": "14844 Bristol Park Blvd",
      "reason_for_recall": "Labeling: Incorrect or Missing Lot and/or Exp Date.",
      "address_2": "",
      "product_quantity": "",
      "code_info": "lot# D001 EXP: 01/02/2018 CPD: 01/02/2019",
      "center_classification_date": "20180629",
      "distribution_pattern": "Nationwide in the USA",
      "state": "OK",
      "product_description": "TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-120-01",
      "report_date": "20180711",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Qualgen, LLC",
      "recall_number": "D-0893-2018",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "80203",
      "termination_date": "20201125",
      "more_code_info": "",
      "recall_initiation_date": "20180608",
      "postal_code": "73013-1891",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}