reVive Light Therapy Pain Relief Device — Class II medical device recall Z-1581-2016
Terminated recall by LED Technologies, LLC, reported 2016-05-04. Incorrect Power Supply in the package, rendering the device inoperable.
| Recall number | Z-1581-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | LED Technologies, LLC, Greenwood Village, CO, United States |
| Recall initiated | 2016-03-30 |
| Classified | 2016-04-27 |
| Reported by FDA | 2016-05-04 |
| Terminated | 2016-11-30 |
| Quantity | 32 units |
| Lot numbers | 1052 |
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.
Reason for recall
Incorrect Power Supply in the package, rendering the device inoperable.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1581-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.