FDA Adverse Event Injury Summary report: N

EYEBOT

MDR report key: 24294831 · Received February 9, 2026

Report

Report Number
MW5183539
Event Type
Injury
Date Received
February 9, 2026
Date of Event
December 20, 2025
Report Date
February 2, 2026
Manufacturer
ZENNI OPTICAL INC.
Product Code
HLN
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

TO WHOM IT MAY CONCERN, I AM WRITING TO FILE A COMPLAINT REGARDING EYEBOT, A COMPANY THAT CLAIMS TO PROVIDE AUTONOMOUS EYEGLASS PRESCRIPTIONS AND EYEWEAR. AFTER RECEIVING A PRESCRIPTION AND EYEGLASSES FROM EYEBOT IN (B)(6), I FOUND THAT THE GLASSES I WAS PROVIDED DID NOT WORK CORRECTLY AND WERE UNUSABLE FOR MY VISION NEEDS. DESPITE HAVING PAID EYEBOT FOR THIS SERVICE, I ULTIMATELY HAD TO VISIT MY OPTOMETRIST AND SPEND ADDITIONAL MONEY OUT OF POCKET TO OBTAIN A CORRECT AND FUNCTIONAL PAIR OF GLASSES. EYEBOT MARKETS ITSELF AS AN AUTONOMOUS EYEGLASS SOLUTION, BUT IN MY EXPERIENCE, THE PRODUCT THEY PROVIDED WAS INACCURATE AND INEFFECTIVE. I AM CONCERNED THAT CONSUMERS ARE BEING MISLED INTO PAYING FOR EYEWEAR THAT DOES NOT MEET PROPER VISION CORRECTION STANDARDS, POTENTIALLY CAUSING FINANCIAL HARM AND VISION-RELATED ISSUES. I BELIEVE THIS PRACTICE IS DECEPTIVE AND WARRANTS REVIEW, AS IT MAY AFFECT PUBLIC TRUST AND CONSUMER SAFETY. I AM SUBMITTING THIS COMPLAINT SO THAT THE FDA CAN EVALUATE EYEBOT'S CLAIMS, PRACTICES, AND THE ACCURACY OF THE EYEWEAR THEY PROVIDE. THANK YOU FOR YOUR TIME AND ATTENTION TO THIS MATTER.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
360085 EYEBOT GAUGE, LENS, OPHTHALMIC HLN ZENNI OPTICAL INC.

Patients

Seq Age Sex Outcome Treatment
1 NA Female Required Intervention