{
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    "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/",
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    "last_updated": "2026-08-20",
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      "reason_for_recall": "Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation",
      "root_cause_description": "Device Design",
      "action": "On December 4, 2017, Accord Media distributed Urgent Medical Device Field Action notices and Response Forms to customers via courier service.  Customers were instructed to inspect stock and identify affected product whereby the would apply a label to the product which reads \"DO NOT USE GREEN LIGHT FUNCTIONALITY - NOT FDA CLEARED FOR USE\".  Customers are encouraged to complete and return the response form via email to: customerservice@truthinaging.com.",
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