NovoTHOR Whole Body Light Pod — Class II medical device recall Z-0972-2024
Ongoing recall by THOR Photomedicine Ltd, reported 2024-02-07, distributed in AZ, CA, CO, CT, FL, GA, HI, ID…. One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a
| Recall number | Z-0972-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | THOR Photomedicine Ltd, Amersham, United Kingdom |
| Recall initiated | 2023-11-20 |
| Classified | 2024-02-01 |
| Reported by FDA | 2024-02-07 |
| Distributed | AZ, CA, CO, CT, FL, GA, HI, ID, IN, MD, NJ, NY, OR, PA, TX, WA, WI |
| Countries outside the US | AE, AU, CA, CH, GB, IT, MT, NO |
| Reason classes | device malfunction |
| UPC / GTIN / UDI-DI | 05060494130503, 05060494130510, 05060494130527 |
| Serial numbers | 4002, 4003, 4004, 4006, 4009, 4010, 4012, 4013, 4014, 4017, 4019, 4021, 4023, 4024, 4026, 4027, 4028, 4029, 4030, 4035, 4037, 4038, 4040, 4042, 4043 and 36 more |
Product
NovoTHOR Whole Body Light Pod, Gen 3.0 (1) Product Code S2188 - Reg (2) Product Code S2189 - Reg PRX (3) Product Code S2190 - XL
Reason for recall
One of the ball studs attaching a gas strut to the canopy may fail. There is potential risk of injury should a ball stud fail when someone is in the NovoTHOR and trying to open or close the canopy
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-0972-2024. 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.