Recall Z-0455-2024— Thor Photomedicine Ltd
Class II · Ongoing
Class II FDA medical device recall by Thor Photomedicine Ltd, initiated 2022-09-13. FDA's recall record names no specific 510(k) clearance for this event. Product: NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183. Reason: Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift..
- Recalling firm
- Thor Photomedicine Ltd
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-09-13
- Firm location
- Chesham, United Kingdom
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.