Tampa, FL, United States
Ottlite TEchnologies, Inc. recalls
1 recall recorded since 2018, most recently on 17 November 2022. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 17 November 2022
- Reason
- 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
- Initiated
- FDA Mandated
- Recall number
- Z-1473-2023
- OttLite Rechargeable UVC Disinfecting Wand
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.