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MAX LUX CORP Recall 89050

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 with an intended use of disinfecting surfaces.

MAX LUX CORP Recall 89050 Information

StatusOngoing
Mandated?FDA Mandated
Recall NumberZ-0246-2022
Event ID89050
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 with an intended use of disinfecting surfaces.
Product TypeDevices
DistributionUS Nationwide Distribution
Quantity9900 units
Recall ReasonExcessive ultraviolet-C radiation
Device Classification20211208
Device Code InfoSafe-T Lite
Center Classification Date20211129
Recall Initiation Date20211026
Recalling FirmMAX LUX CORP
Initial Notification Letter
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