{
  "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": {
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  "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: C243 BUD: 11/21/2018; D010 BUD: 1/11/2019; D025 BUD: 1/30/2019",
      "center_classification_date": "20181107",
      "distribution_pattern": "Nationwide.",
      "state": "OK",
      "product_description": "Testosterone 87.5mg pellet, 1 count (NDC 69761-187-01), 6 count (NDC 69761-187-06), 12 count (NDC 69761-187-12), and 30 count (NDC 69761-187-30) vials, Rx Only Qualgen,  LLC, Edmond, OK 73013",
      "report_date": "20181114",
      "classification": "Class II",
      "openfda": {},
      "recalling_firm": "Qualgen, LLC",
      "recall_number": "D-0237-2019",
      "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"
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}