{
  "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,
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  "results": [
    {
      "status": "Terminated",
      "city": "Daytona Beach",
      "state": "FL",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "80750",
      "recalling_firm": "Product Quest Manufacturing LLC",
      "address_1": "330 Carswell Ave",
      "address_2": "N/A",
      "postal_code": "32117-4416",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide in the USA",
      "recall_number": "D-0027-2019",
      "product_description": "DERMATONE (titanium oxide 6% and zinc oxide 4.7%) No-Touch Sunscreen Stick, SPF 50, Net Wt. 0.49 oz. (13.9g) stick, Distributed by: Beaumont Products, Inc. Kennesaw, GA 30144, UPC 0 20908 05100 3.",
      "product_quantity": "5025 sticks",
      "reason_for_recall": "Microbial Contamination of Non-Sterile Products: sample tested positive for Staphylococcus aureus.",
      "recall_initiation_date": "20180803",
      "center_classification_date": "20181016",
      "termination_date": "20210330",
      "report_date": "20181024",
      "code_info": "Lot: 172428G"
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}