FDA Device recall Z-0454-2024
G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
- FDA Device
- Class II
- ongoing
- Published 2023-12-13
On 2023-12-13 the FDA classified a Class II recall of G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177 by Thor Photomedicine, citing failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0454-2024 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2022-09-13 |
| Published | 2023-12-13 |
| Last updated | 2026-09-13 11:56 UTC |
| Company | Thor Photomedicine |
| Distribution | US |
Product
G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
Reason
Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.
Identifiers
| code_info | Serial numbers: 3001, 3002, 3004, 3008, 3009, 3006, 3003. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0454-2024%22
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