Class II — Thor Photomedicine Ltd
| Recalling firm | THOR Photomedicine Ltd |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift. |
| Product | G041 POD, THOR NOVO GEN 2.0 XL whole body red light therapy bed, model S1177 |
| Quantity | 6 |
| Distribution | Worldwide Distribution: US (Nationwide): Arizona, California, Colorado, Connecticut, Florida, Hawaii, Idaho, Illinois, Iowa, Maryland, Michigan, Minnesota, Missouri, Nevada, New Hampshire, North Carolina, Ohio, Oregon, Texas, Utah, Virginia, West Virginia. OUS (foreign) to countries of: Australia, Canada, Netherlands, New Zealand, Singapore, United Kingdom. |
| Initiated | 2022-09-13 |
| Classified | 2023-12-01 |
| Recall number | Z-0454-2024 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Thor Photomedicine Ltd (Z-0454-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/93344/
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