FDA Recall
Open, Classified
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Recall: Z-1661-2022
·
Initiated August 1, 2022
Recall
- Recall Number
- Z-1661-2022
- Event Number
- 90799
- Firm
- MERCHSOURCE LLC
- FEI Number
- 3014733988
- Product Code
- RHP
- Status
- Open, Classified
- Root Cause
- Radiation Control for Health and Safety Act
- Initiated
- August 1, 2022
- Address
- 7755 Irvine Center Dr, Irvine, CA, 92618-2906
Description
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Reason
Excessive ultraviolet-C radiation
Action
MerchSource issued a Safety Recall letter to affected customers dated August, 2022. Customers were instructed to immediately terminate sale of the Sharper Image UV Sanitizing Portable Wand MerchSource will coordinate with you for the return or destruction of the product. MerchSource will provide a refund in the full amount of the purchase price to all of its customers affected.
Distribution
US Nationwide Distribution