Reported May 4, 2016 · Terminated

reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain Relief…

LED Technologies, LLC

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: LED Technologies, LLC · 6000 Greenwood Plaza Blvd · Greenwood Village, CO · 80111-4816

Is this the product you have?

  • reVive Light Therapy
  • Pain Relief Device (Model NumberRVPNSYS)
  • Product UsageThe 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
Lot codes and dates
  • Manufactured between 12/15/2015 and 12/28/2015 for specific lot #1052
Amount recalled
32 units

Why it was recalled

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

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Notice updated Nov 30, 2016 · Data as of Sep 19, 6:05 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.