{
  "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,
      "limit": 1,
      "total": 1
    }
  },
  "results": [
    {
      "status": "Terminated",
      "city": "Plano",
      "state": "TX",
      "country": "United States",
      "classification": "Class II",
      "openfda": {},
      "product_type": "Food",
      "event_id": "62872",
      "recalling_firm": "Drucker Labs LP",
      "address_1": "1600 Capital Ave Ste 100",
      "address_2": "N/A",
      "postal_code": "75074-8187",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide and to Canada",
      "recall_number": "F-2126-2012",
      "product_description": "intraKID Lot 658 with a Best By date of 12/12, 33 oz and 2 oz bottles",
      "product_quantity": "2026 bottles",
      "reason_for_recall": "After extensive testing and investigation, Drucker Labs has determined that an incorrect form of Vitamin B3, Nicotinic Acid, was used in the manufacturing of intraKID Lot 658.  This nutrient may cause a temporary symptom in a small number of consumers.  This symptom, commonly known as \u001cNiacin Flush,\u001d may include itching, redness, or warmth of the skin.  This typically subsides within 15 \u0013 20 minut",
      "recall_initiation_date": "20120813",
      "center_classification_date": "20120905",
      "termination_date": "20141007",
      "report_date": "20120912",
      "code_info": "Lot 658 with a Best By date of 12/12"
    }
  ]
}