Drug recall
reVive Light Therapy Pain Relief Device (Model Number: RVPNSYS) Product Usage: The reVive Light Therapy Pain…
FDA recall event 73779 · Class II · LED Technologies, LLC
Key facts
| Event ID | 73779 |
|---|---|
| Recall numbers | Z-1581-2016 |
| Recalling firm | LED Technologies, LLC |
| Product type | Devices |
| 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… |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Incorrect Power Supply in the package, rendering the device inoperable. |
| Initiation date | Mar 30, 2016 |
| Report date | May 4, 2016 |
| Termination date | Nov 30, 2016 |
| City | Greenwood Village |
| State | CO |
| Country | United States |
| FEI number | 3006315288 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: