Recall Z-1473-2023— Ottlite TEchnologies, Inc.
Class II · Ongoing
Class II FDA medical device recall by Ottlite TEchnologies, Inc., initiated 2022-11-17. FDA's recall record names no specific 510(k) clearance for this event. Product: OttLite Rechargeable UVC Disinfecting Wand. 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..
- Recalling firm
- Ottlite TEchnologies, Inc.
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2022-11-17
- Firm location
- Tampa, FL, United States
Product description
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.
Data sourced from openFDA. This site is unofficial and independent of the FDA.