Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Recalled by LED Technologies, LLC Due to Incorrect Power Supply in the package, rendering the...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact LED Technologies, LLC directly.
Affected Products
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.
Quantity: 32 units
Why Was This Recalled?
Incorrect Power Supply in the package, rendering the device inoperable.
Where Was This Sold?
Distributed to 1 consignee located in the United States.
About LED Technologies, LLC
LED Technologies, LLC has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report