FDA Medical Device Recalls (openFDA)
Ottlite TEchnologies, Inc.: OttLite Rechargeable UVC Disinfecting Wand
- Recall number
- Z-1473-2023
- Recalling firm
- Ottlite TEchnologies, Inc.
- Product
- OttLite Rechargeable UVC Disinfecting Wand
- Status
- Open, Classified
- Initiated
- 2022-11-17
- Posted
- 2023-05-01
- Terminated
- not on file
- 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.
- Root cause
- Radiation Control for Health and Safety Act
- Action
- 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.
- Quantity
- 7376 units
- Distribution
- US Natioonwide Distribution
- Lot, serial or model codes
- model: UV10002M
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- RHP
- Firm FEI
- 1000132325
- Firm city
- Tampa
- Firm state
- FL
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28