FDAClass IIDecember 13, 2023

NovoTHOR Gen 2.0 whole body red light therapy bed recall

NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176

Why was NovoTHOR Gen 2.0 whole body red light therapy bed recalled?

Failure of ball stud components causing the gas strut on one side to detach from the canopy, making the canopy difficult to lift.

What should I do if I have this product?

The recall is ongoing. Follow the firm and FDA instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

Serial numbers: 2003, 2004, 2005, 2006, 2007, 2009, 2010, 2011, 2017, 2018, 2015, 2020, 2019, 2001, 2021, 2028, 2033, 2036, 2030, 2029.

Product
NovoTHOR Gen 2.0 whole body red light therapy bed, model S1176
Recalling firm
Thor Photomedicine Ltd
Quantity
19
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.
Recall date
December 13, 2023
Classification
Class II
Status
Ongoing
Agency
FDA (device)
Open FDA enforcement record Latest recalls