Ottlite TEchnologies, Inc. OttLite Rechargeable UVC Disinfecting Wand Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
OttLite Rechargeable UVC Disinfecting Wand
Brand
Ottlite TEchnologies, Inc.
Lot Codes / Batch Numbers
model: UV10002M
Products Sold
model: UV10002M
Ottlite TEchnologies, Inc. is recalling OttLite Rechargeable UVC Disinfecting Wand due to Product allows for the emission of ultraviolet (UV) electronic product radiation in excess of exposure limits recommended by the International Commiss. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
OttLite, sent consumers a Notification letter. The letter identified the affected product, problem and actions to be taken. Consumers should immediately stop using the recalled product and return the item to OttLite to receive a replacement product. The letter provided instructions for returning your OttLite Rechargeable UVC Disinfecting Wand (model: UV10002M) to Ottlite. 1. Go to our website at: www.OttLite.com/Recall 2. Fill out the form at the website including letting us know if you still have the UV10002M UV Wand in your possession. 3. Copy your purchase receipt and submit it on the website form. a. We will contact you and send a postage paid return envelope to return the wand if you still have it in your possession. 4. Once OttLite receives the consumer s information, we will ship a replacement Ottlite UVC Disinfecting Phone Case with Wireless Charging to the address you entered in the website.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026