Accord Media recalls Ultra Renew Plus devices due to unapproved green LED light used for hyperpigmentation treatment. Consumers should check if they own this device and follow official instructions.
Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation
Accord Media is recalling Ultra Renew Plus devices because they contain an unapproved green LED light intended for hyperpigmentation treatment. This poses a risk as the device was not approved by medical authorities for this use.
The device uses a green LED light that was not approved by medical authorities for treating hyperpigmentation. This unapproved use could lead to unintended health effects if the device is used without proper medical supervision.
People who own or use Ultra Renew Plus devices for hyperpigmentation treatment are affected. Those with medical conditions requiring light therapy may be at higher risk.
Check for Ultra Renew Plus devices with unapproved green LED lights used for hyperpigmentation treatment. The product has no specific model numbers or dates listed in the recall notice.
Look for Ultra Renew Plus devices with unapproved green LED lights used for hyperpigmentation treatment.
The recall states the device uses an unapproved green LED light for hyperpigmentation treatment, so it is not approved by medical authorities for this use.
The recall does not specify a remedy, so check with Accord Media for further instructions.
The recall record does not list specific model numbers or dates for the affected devices.
We’ve drafted a message you can send Accord Media to request your refund or repair — edit it as you like.
Subject: Recall Z-0821-2018 — Accord Media Accord Media Hello, I own a Accord Media that is covered by recall Z-0821-2018 from Accord Media. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
