NovoTHOR Gen 2.5 Regular whole body red light therapy recall
NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
Why was NovoTHOR Gen 2.5 Regular whole body red light therapy 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: 2002, 2050, 2051, 2052, 2053, 2054, 2055, 2056, 2057, 2059, 2060, 2061, 2062, 2064, 2065, 2066, 2075, 2076, 2077, 2078, 2081, 2084, 2085, 2086, 2088, 2089, 2090, 2094, 2097.
- Product
- NovoTHOR Gen 2.5 Regular whole body red light therapy bed, model S2183
- Recalling firm
- Thor Photomedicine Ltd
- Quantity
- 26
- 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)