{
  "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": {
      "skip": 0,
      "limit": 1,
      "total": 1
    }
  },
  "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": "NDC 44118-809-30; 747 and NDC 76331-807-30; 1493",
      "code_info": "NDC 44118-809-30; Lot 40614B, exp. 9/14 and   NDC 76331-809-30; lot 39736A, exp. 3/2014,",
      "center_classification_date": "20130816",
      "distribution_pattern": "Nationwide.",
      "state": "GA",
      "product_description": "Duet DHA 400 ec, containing one 30-count bottle of multi-vitamin tablets (imprinted 800) and one 30-count bottle of Omega-3 softgel capsules, Rx only, Manufactured for Eckson Labs, Wilmington, DE (NDC 44118-809-30) and Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-809-30)",
      "report_date": "20130828",
      "classification": "Class III",
      "openfda": {},
      "recalling_firm": "Stayma Consulting Service, LLC.",
      "recall_number": "D-896-2013",
      "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"
    }
  ]
}