FDA recall Z-1473-2023

Ottlite TEchnologies, Inc. · Class II · device

Product

OttLite Rechargeable UVC Disinfecting Wand

Reason for recall

Product allows for the emission of ultraviolet (UV) electronic product radiation in excess of exposure limits recommended by the International Commission on Non-ionizing Radiation Protection (ICNIRP). The emissions are hazardous to users and others in the vicinity.

Distribution

US Natioonwide Distribution

Key facts

Status: Ongoing
Initiation date: 2022-11-17
Report date: 2023-05-10
Voluntary/Mandated: FDA Mandated
Location: Tampa, FL, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1473-2023