{
  "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": "2026-04-01",
    "results": {
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  "results": [
    {
      "country": "United States",
      "city": "Suwanee",
      "address_1": "5400 Laurel Springs Pkwy",
      "reason_for_recall": "Subpotent; Beta carotene (Vitamin A)",
      "address_2": "Suite 803",
      "product_quantity": "2985",
      "code_info": "NDC 76331-808-30; lot 39736A, exp. 3/14 and lot 41667, exp. 12/14",
      "center_classification_date": "20130816",
      "distribution_pattern": "Nationwide.",
      "state": "GA",
      "product_description": "Duet DHA 430, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Manufactured for W.H. Nutritionals, Wilmington, DE --- NDC 76331-808-30",
      "report_date": "20130828",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Stayma Consulting Service, LLC.",
      "recall_number": "D-898-2013",
      "initial_firm_notification": "Letter",
      "product_type": "Drugs",
      "event_id": "65663",
      "termination_date": "20140527",
      "recall_initiation_date": "20130628",
      "postal_code": "30024-6056",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "status": "Terminated"
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