FDAClass IIMarch 7, 2018

Ultra Renew Plus recall

Ultra Renew Plus

Why was Ultra Renew Plus recalled?

Distribution of medical devices with unapproved green LED light used to treat hyperpigmentation

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

none

Product
Ultra Renew Plus
Recalling firm
Accord Media, LLC
Quantity
1040 units
Distribution
US Nationwide
Recall date
March 7, 2018
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls