{
  "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": [
    {
      "status": "Terminated",
      "city": "Suwanee",
      "state": "GA",
      "country": "United States",
      "classification": "Class III",
      "openfda": {},
      "product_type": "Drugs",
      "event_id": "65663",
      "recalling_firm": "Stayma Consulting Service, LLC.",
      "address_1": "5400 Laurel Springs Pkwy",
      "address_2": "Suite 803",
      "postal_code": "30024-6056",
      "voluntary_mandated": "Voluntary: Firm initiated",
      "initial_firm_notification": "Letter",
      "distribution_pattern": "Nationwide.",
      "recall_number": "D-895-2013",
      "product_description": "Duet DHA 400, 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 44118-807-30) --- Also Manufactured for W.H. Nutritionals, Wilmington, DE (NDC 76331-807-30)",
      "product_quantity": "1,460 and 2,990",
      "reason_for_recall": "Subpotent; Beta carotene (Vitamin A)",
      "recall_initiation_date": "20130628",
      "center_classification_date": "20130816",
      "termination_date": "20140527",
      "report_date": "20130828",
      "code_info": "NDC 44118-807-30 Lots 40614, exp. 9/14 and 40614A, exp. 9/14    NDC 76331-807-30 lot 39736A, exp. 3/2014, and lot 41667, exp. 12/2014"
    }
  ]
}