Z-1473-2023 Class II Ongoing
FDA device recall Z-1473-2023 was initiated by Ottlite TEchnologies, Inc. on November 17, 2022 and is designated Class II. 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 recall status is ongoing. Affected quantity: 7376 units.
Recall Details
- Product Type
- Devices
- Report Date
- May 10, 2023
- Initiation Date
- November 17, 2022
- Termination Date
- N/A
- Voluntary/Mandated
- FDA Mandated
- Product Quantity
- 7376 units
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.
Distribution Pattern
US Natioonwide Distribution
Code Information
model: UV10002M