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.

Recall Insight

This FDA Devices action (record #Z-1581-2016) was formally reported on May 4, 2016, with the manufacturer initiating the action on March 30, 2016. It is classified under Moderate severity (Class II), with a current status of Terminated. Led Technologies, LLC is listed as the recalling firm, operating out of Greenwood Village, CO. Federal records indicate 32 units units are affected.

The documented reason for this recall is: Incorrect Power Supply in the package, rendering the device inoperable. Distribution data in the federal record shows the product reached: Distributed to 1 consignee located in the United States.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.

To put this record in context, PlainRecalls indexes 83,949 recalls across the FDA, CPSC and NHTSA going back to 1995. Within the same product category, the database holds 6 closely related recalls, of which 6 were also issued by FDA Devices. That clustering is a signal — repeated actions in a narrow category often indicate a systemic quality-control issue, a supplier-wide contamination, or a design defect that has propagated across product lines. This recall is roughly 10 years old; older recalls can remain relevant because many units enter resale, rental, and secondary-market channels where the original warning never reaches the end user. Always cross-check the recall number against the official agency page before relying on any summary.