LED Technologies, LLC: Medical Device Recall in 2016 - (Recall #: Z-1581-2016)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2016.

Data Source: FDA.

Product Description:

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.

Product Classification:

Class II

Date Initiated: March 30, 2016

Date Posted: May 4, 2016

Recall Number: Z-1581-2016

Event ID: 73779

Reason for Recall:

Incorrect Power Supply in the package, rendering the device inoperable.

Status: Terminated

Product Quantity: 32 units

Code Information:

Manufactured between 12/15/2015 and 12/28/2015 for specific lot #1052

Distribution Pattern:

Distributed to 1 consignee located in the United States.

Voluntary or Mandated:

Voluntary: Firm initiated