{
  "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": "2026-04-01",
    "results": {
      "skip": 0,
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  "results": [
    {
      "status": "Ongoing",
      "city": "Marietta",
      "state": "GA",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Devices",
      "event_id": "92735",
      "recalling_firm": "Advance Medical Designs, Inc.",
      "address_1": "1241 Atlanta Industrial Dr",
      "address_2": "",
      "postal_code": "30066-6606",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit",
      "distribution_pattern": "US, Canada, UK, Panama, Netherlands",
      "recall_number": "Z-2533-2023",
      "product_description": "50-GEL20; Ultrasound gel",
      "product_quantity": "13750 units",
      "reason_for_recall": "Ultrasound gel mislabeled with inappropriate use.",
      "recall_initiation_date": "20230707",
      "center_classification_date": "20230908",
      "report_date": "20230920",
      "code_info": "Lot Number 21043C2328",
      "more_code_info": ""
    }
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}