FDAFDA · Food and drugs·Recall number Z-1581-2016
reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain Relief Device is a device designed to deliver LED light spectrum in 880nm and 660nm directly into the body tissue to increase circulation and temporarily relieve pain associated with muscle spasms, arthritis, general aches and strains.
Published May 4, 2016 · Recall initiated: March 30, 2016
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Incorrect Power Supply in the package, rendering the device inoperable.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- LED Technologies, LLC
- Distributor
- Distributed to 1 consignee located in the United States.
- Lot
- Manufactured between 12/15/2015 and 12/28/2015 for specific lot #1052
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.