{
  "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": {
      "skip": 0,
      "limit": 1,
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  },
  "results": [
    {
      "status": "Terminated",
      "city": "Rosenberg",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "93986",
      "recalling_firm": "Seatex LLC",
      "address_1": "445 Highway 36 N",
      "address_2": "",
      "postal_code": "77471-8756",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "E-Mail",
      "distribution_pattern": "Nationwide in the US and Puerto Rico",
      "recall_number": "D-0357-2024",
      "product_description": "PROBLEND E3 Foaming Hand Sanitizer, All-In-One Foaming Hand Sanitizer & Cleanser, Seatex LLC, 445 TX Hwy 36 Rosenberg, TX 77471",
      "product_quantity": "274 cases",
      "reason_for_recall": "CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.",
      "recall_initiation_date": "20240219",
      "center_classification_date": "20240229",
      "termination_date": "20250815",
      "report_date": "20240306",
      "code_info": "Lot #: 265029, Exp. 03/27/2024; 273759, Exp. 11/29/2024.",
      "more_code_info": ""
    }
  ]
}