Drug recall
G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
FDA recall event 93344 · Class II · Thor Photomedicine Ltd
Key facts
| Event ID | 93344 |
|---|---|
| Recall numbers | Z-0453-2024, Z-0454-2024, Z-0455-2024, Z-0456-2024 |
| Recalling firm | Thor Photomedicine Ltd |
| Product type | Devices |
| Products | G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177, NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176, NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183, NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184. |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift. |
| Initiation date | Sep 13, 2022 |
| Report date | Dec 13, 2023 |
| City | Chesham |
| Country | United Kingdom |
| FEI number | 3003899624 |
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: