Class II — LED Technologies, LLC
| Recalling firm | LED Technologies, Inc. |
|---|---|
| Registered facility | LED TECHNOLOGIES, INC. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | Incorrect Power Supply in the package, rendering the device inoperable. |
| Product | 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 |
| Distribution | Distributed to 1 consignee located in the United States. |
| Initiated | 2016-03-30 |
| Classified | 2016-04-27 |
| Terminated | 2016-11-30 |
| Recall number | Z-1581-2016 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — LED Technologies, LLC (Z-1581-2016).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/73779/
Alerts for LED Technologies, Inc.
Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.
Want a one-page facility brief?
A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.