[Recalled] NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183 — Failure of ball stud components causing the gas strut on one side to detach fro… | FDA 2022-09-13

A safety authority has issued a recall or warning for this item. The confirmed facts from the source notice are laid out below.

Recall details

Why it was recalled

According to the FDA_DEVICE notice, the identified hazard is: Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.

This Class II recall concerns device products distributed in United Kingdom and was recorded by FDA_DEVICE. Recalls in this category are published so that owners, retailers, and importers can identify affected units and act quickly.

What to do if you own this product

Check whether your unit is affected and follow the authority's guidance before further use.

Read the full official notice →

Related recalls from Thor Photomedicine Ltd

• NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176 — Class II

This page indexes a public government recall notice for reference. We do not sell or verify this product; always confirm the current status on the authority's official site.