{
  "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": "2026-06-17",
    "results": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Ongoing",
      "city": "Winder",
      "state": "GA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Food",
      "event_id": "97884",
      "recalling_firm": "Winder Laboratories, LLC",
      "address_1": "716 Patrick Industrial Ln",
      "address_2": "N/A",
      "postal_code": "30680-8333",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Product was shipped to the following states: AL, AZ, CA, FL, HI, IA, IL, IN, MA, MI, MO, MS, NC, NJ, NY, OR, PA, PR, RI, TN, TX, UT, WA, WI & WV.",
      "recall_number": "H-0569-2026",
      "product_description": "Multivitamin with Fluoride Chewable Tablets Grape Flavor Rx NDC 75826-169-10 0.25 mg 100 TABLETS UPC 3 15826 16910 2; NDC 75826-171-10 1mg 100 TABLETS UPC 3 15826 17110 5 Manufactured by: WINDER LABORATORIES LLC Winder, GA 30680",
      "product_quantity": "422cs/12/0.25mg/100ct bottles + 210cs/12/1.0mg/100ct bottles",
      "reason_for_recall": "Subpotent. During an FDA inspection it was discovered that the product was subpotent for Vitamin D.",
      "recall_initiation_date": "20251027",
      "center_classification_date": "20260313",
      "report_date": "20260325",
      "code_info": "Lot 1692303 SN: 138909557498 EXP: 2025-10-26 & Lot 1692304 SN 131163901709 EXP: 2025-10-26; LOT 1712301 SN: 163590222021 EXP: 2025-11-14",
      "more_code_info": ""
    }
  ]
}