# FDA recall Z-0455-2024

> **Thor Photomedicine Ltd** · Class II · device recall initiated 2022-09-13.

## Product

NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183

## 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.

## 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.

## Key facts

- **Recall number:** Z-0455-2024
- **Recalling firm:** Thor Photomedicine Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-13
- **Report date:** 2023-12-13

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Chesham, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0455-2024

## Citation

> AI Analytics. FDA recall Z-0455-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0455-2024. Source: US FDA. Licensed CC0.

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