FDA Adverse Event Malfunction Summary report: N

ACUVUE OASYS BIWEEKLY

MDR report key: 22938675 · Received September 2, 2025

Report

Report Number
MW5175469
Event Type
Malfunction
Date Received
September 2, 2025
Date of Event
June 1, 2025
Report Date
August 26, 2025
Manufacturer
JOHNSON & JOHNSON VISION CARE, INC.
Product Code
LPM
Product Problem
Yes
Report Source
Voluntary report
Reporter Occupation
PATIENT
Health Professional
*

Narratives

Description of Event or Problem · 0

ACUVUE OASYS BIWEEKLY BY JOHNSON & JOHNSON VISION CARE, INC. ARE BLURRY WITH FIRST USE. THESE ARE SUPPOSED TO LAST TWO WEEKS AND THEY DON'T EVEN LAST 24 HOURS. I HAVE NOTICED THIS WITH THE NEW TEAL PACKAGING.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
2332339 ACUVUE OASYS BIWEEKLY LENSES, SOFT CONTACT, EXTENDED WEAR LPM JOHNSON & JOHNSON VISION CARE, INC.

Patients

Seq Age Sex Outcome Treatment
1 33 YR Female