reVive Light Therapy Pain Relief Device recall
reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain Relief Device is a device designed to…
Why was reVive Light Therapy Pain Relief Device recalled?
Incorrect Power Supply in the package, rendering the device inoperable.
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?
Manufactured between 12/15/2015 and 12/28/2015 for specific lot #1052
- Product
- reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain Relief Device is a device designed to…
- Recalling firm
- LED Technologies, LLC
- Quantity
- 32 units
- Distribution
- Distributed to 1 consignee located in the United States.
- Recall date
- May 4, 2016
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)