FDA Adverse Event
Injury
Summary report: N
RXSIGHT CONTACT LENS
MDR report key: 24006983
·
Received January 8, 2026
Report
- Report Number
- MW5181949
- Event Type
- Injury
- Date Received
- January 8, 2026
- Report Date
- January 7, 2026
- Manufacturer
- RXSIGHT INC.
- Product Code
- HJK
- Adverse Event
- Yes
- Report Source
- Voluntary report
- Reporter Location
- TN, US
- Reporter Occupation
- PATIENT
- Health Professional
- *
Narratives
Description of Event or Problem · 0
I WOULD LIKE TO REPORT A NEGATIVE EXPERIENCE WITH MY RX SIGHT LAL+ LENSES. I HAD THEM INSTALLED (B)(6) 2025 AND AFTER 3 ADJUSTMENTS AND LOCK-INS MY VISION IS BLURRY.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 63434 | RXSIGHT CONTACT LENS | LENS, CONTACT, POLYMETHYLMETHACRYLATE, DIAGNOSTIC | HJK | RXSIGHT INC. |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | NA | Unknown |