G041 POD — Class II medical device recall Z-0454-2024
Ongoing recall by Thor Photomedicine Ltd, reported 2023-12-13, distributed nationwide. Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy
| Recall number | Z-0454-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Thor Photomedicine Ltd, Chesham, United Kingdom |
| Recall initiated | 2022-09-13 |
| Classified | 2023-12-01 |
| Reported by FDA | 2023-12-13 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CA, GB, NL, NZ, SG |
| Quantity | 6 |
| Reason classes | device malfunction |
| Serial numbers | 3001, 3002, 3003, 3004, 3006, 3008, 3009 |
| Model numbers | 1177 |
Product
G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0454-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.