{
  "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": "Lack of Assurance of Sterility",
      "address_2": "",
      "product_quantity": "",
      "code_info": "Lots: C245 BUD: 11/28/2018; D005 BUD: 1/5/2019; D027 BUD: 1/31/2019; D035 BUD: 2/9/2019; D058 BUD: 3/9/2019",
      "center_classification_date": "20181107",
      "distribution_pattern": "Nationwide.",
      "state": "OK",
      "product_description": "Testosterone 37.5 mg pellet, 1 count (NDC 69761-137-01), 6 count (NDC 69761-137-06), 12 count (NDC 69761-137-12) and 30 count (NDC 69761-137-30) vials, Rx Only, Qualgen, LLC, Edmond, OK 73013",
      "report_date": "20181114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Qualgen, LLC",
      "recall_number": "D-0235-2019",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "81346",
      "termination_date": "20200604",
      "more_code_info": "",
      "recall_initiation_date": "20181017",
      "postal_code": "73013-1891",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
    }
  ]
}