{
  "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": "2026-07-22",
    "results": {
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  "results": [
    {
      "status": "Ongoing",
      "city": "Elmsford",
      "state": "NY",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "96981",
      "recalling_firm": "Advanced Pharmaceutical Technology, Inc.",
      "address_1": "132 S Central Ave",
      "address_2": "",
      "postal_code": "10523-3509",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "NY, NJ",
      "recall_number": "D-0531-2025",
      "product_description": "TESTO-200, Testosterone Cypionate Inj. USP, 2000mg/10ml (200mg/ml), One 10ml multidose vial per carton, For intramuscular injection only, Rx Only, ADVANCED PHARMACEUTICAL TECHNOLOGY, INC., 132 South Central Avenue, Elmsford, NY 10523.  NDC 57377-200-01",
      "product_quantity": "26 vials",
      "reason_for_recall": "Marketed Without an Approved NDA/ANDA",
      "recall_initiation_date": "20250530",
      "center_classification_date": "20250716",
      "report_date": "20250702",
      "code_info": "Lot P-24-1; Exp. 02/28/2027",
      "more_code_info": ""
    }
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}