FDA Adverse Event Malfunction Summary report: N

BOARD STIFF PROGRESSIVE READERS +250 MAGNIFICATION

MDR report key: 23839165 · Received December 18, 2025

Report

Report Number
MW5180811
Event Type
Malfunction
Date Received
December 18, 2025
Report Date
December 11, 2025
Manufacturer
EYEBOBS, LLC.
Product Code
HOI
Product Problem
Yes
Report Source
Voluntary report
Reporter Location
IL, US
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

I WAS GIFTED A PAIR OF EYEBOBS BOARD STIFF IN BROWN SUGAR PROGRESSIVE READERS IN +250 MAGNIFICATION. AFTER LESS THAN TWO WEEKS OF USE THE LENS KEPT POPPING OUT AND ALTHOUGH I COULD PLACE IT BACK IN THE PROBLEM WAS PERSISTENT. I CONTACTED (B)(6) CUSTOMER SERVICE SEEKING ASSISTANCE IN THIS MATTER AND WAS SUGGESTED BY THEM I PURCHASE NEW LENSES. I THEN EXPLAINED THAT I TOOK THE GLASSES TO AN OPTICAL SHOP AND WAS TOLD THERE WAS A DEFECT IN THE LENS GROOVE AND THEY COULD NOT BE REPAIRED. THEY HAVE REPLIED SINCE I COULD NOT PROVIDE PROOF OF PURCHASE WHICH I AM UNABLE TO DO AS THEY WERE A GIFT THROUGH A SENIOR CENTER AND I DO NOT KNOW WHO TOOK MY NAME WITH A LIST OF ITEMS I COULD USE NOR DOES THE CENTER KNOW AS NAMES ARE GIVEN TO PEOPLE WHO PURCHASE A GIFT AND GIVE IT ANONYMOUSLY BACK TO THE CENTER TO GIVE TO US. THEN I COULD SEND THEM TO THEM AND THEY WOULD SEE IF THEIR IN-HOUSE OPTICAL COULD REPAIR THEM WHICH I ALREADY KNEW WAS NOT POSSIBLE. AFTER LOOKING AT REVIEWS, I FOUND A THEME OF REPLACE THE LENSES, ISSUES HONORING THE WARRANTY, POOR QUALITY AND TERRIBLE CUSTOMER SERVICE. I DID NOT REQUEST THIS BRAND OR ANY BRAND BUT IT APPEARS THAT THERE ARE PROBLEMS WITH THEIR NON-PRESCRIPTION READERS AND SUCH PRODUCTS ARE CLASSIFIED AS CLASS 1 MEDICAL DEVICES.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2282198 BOARD STIFF PROGRESSIVE READERS +250 MAGNIFICATION SPECTACLE, MAGNIFYING HOI EYEBOBS, LLC.

Patients

Seq Age Sex Outcome Treatment
1 75 YR Female