Drug recall
EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very broadband light source emitting…
FDA recall event 84378 · Class II · Energetiq Technology Inc
Key facts
| Event ID | 84378 |
|---|---|
| Recall numbers | Z-0870-2020 |
| Recalling firm | Energetiq Technology Inc |
| Product type | Devices |
| Products | EQ-400-RH-QZ and EQ-400-LH-BK products Product Usage: The device is a very broadband light source emitting incoherent non-laser light from the Deep UV through the visible wavelengths. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | FDA Requested |
| Reason for recall | On September 27, 2019 Energetiq Technology (the manufacturer) discovered a problem with their EQ-400-RH-QZ and EQ-400-LH-BK products during routine manufacturing functional testing. It was noted that… |
| Initiation date | Sep 27, 2019 |
| Report date | Feb 5, 2020 |
| City | Woburn |
| State | MA |
| Country | United States |
| FEI number | 3006791375 |
At a glance
- 1–9 Products in this recall
- None 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: