{
  "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,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Athens",
      "state": "TN",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "90756",
      "recalling_firm": "Midlab Incorporated",
      "address_1": "140 Private Brand Way",
      "address_2": "",
      "postal_code": "37303-1401",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Naionwide within the United States",
      "recall_number": "D-1463-2022",
      "product_description": "Maxim Instant Foam Hand Sanitizer (benzalkonium chloride 0.1%) packaged in a) 1 U.S. Gallon (3.78 Liters) drums UPC 7 61841 02502 6 and b) 55 U.S. Gallon drums (208 Liters) UPC 0 07 61841 02504 0, Midlab 140 Private Brand Way, Athens, TN 37303",
      "product_quantity": "892 gallons and one 55-gallon drum",
      "reason_for_recall": "CGMP Deviations: Product manufactured using expired active ingredient, Benzalkonium chloride.",
      "recall_initiation_date": "20220808",
      "center_classification_date": "20220825",
      "termination_date": "20230815",
      "report_date": "20220831",
      "code_info": "Lot #: a) 03292022-1, 05092022-1, 02012022-1, 06172022-1, 12132021-1, 07272022-1, and b) 06252022-1",
      "more_code_info": ""
    }
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}