FDA Device recall Z-0456-2024
NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184
- FDA Device
- Class II
- ongoing
- Published 2023-12-13
On 2023-12-13 the FDA classified a Class II recall of NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184 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-0456-2024 |
| 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
NovoTHOR Gen 2.5 XL whole body red light therapy bed, model S2184.
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: 3025, 3026, 3027, 3030, 3031, 3034, 3035, 3036, 3037, 3038, 3039, 3040, 3042, 3043, 3044, 3045, 3047, 3050, 3051, 3053. |
|---|
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-0456-2024%22
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