Product Safety Recalls

Product Recall Tracker

MERCHSOURCE LLC Recall 90799

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.

MERCHSOURCE LLC Recall 90799 Information

StatusOngoing
Mandated?FDA Mandated
Recall NumberZ-1661-2022
Event ID90799
Event DescriptionThe 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.
Product TypeDevices
DistributionUS Nationwide Distribution
Recall ReasonExcessive ultraviolet-C radiation
Device Classification20220914
Device Code Infomodel no. 1013622
Center Classification Date20220906
Recall Initiation Date20220801
Recalling FirmMERCHSOURCE LLC
Initial Notification Letter
Similar To

© 2022 Recall.Report / Contact / Privacy Policy

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied.
Recall.report is not affiliated with the Consumer Product Safety Commision, FDA, or US government in any way.