Light Adjustable Lens (LAL) 60007-0070Recalls & reported problems
Rxsight, Inc. · LAL+, Light Adjustable Lens, Sterile, Packaged, 7.0 Diopter · Class 3 · Implant
All models of Light Adjustable Lens (LAL) (33)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00818806021408), received between Apr 14, 2026 and Apr 14, 2026 — classified as 1 injury.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Blurred Vision1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 14, 2026Adverse Event Without Identified Device or Use Problem
A SITE REPORTED TO RXSIGHT THAT A PATIENT'S LIGHT ADJUSTABLE LENS+ (LAL+) WAS EXPLANTED FROM THE RIGHT EYE DUE TO BLURRY NEAR VISION. A LIGHT ADJUSTABLE LENS (LAL) WAS IMPLANTED AS A REPLACEMENT. THE PATIENT EXPERIENCED POST-OPERATIVE WOUND ISSUES, WHICH ARE BEING ADDRESSED IN A SEPARATE MEDWATCH REPORT (SEE H10). AFTER THE WOUND ISSUES WERE ADDRESSED, THE PATIENT'S VISION WAS REPORTED TO HAVE IMPROVED. NO ADDITIONAL INFORMATION IS AVAILABLE.
Patient problems: Blurred Vision
MAUDE report 24879779 ↗
Other Light Adjustable Lens (Lal) And Light Delivery Device (Ldd) devices
- RxSight Light Adjustable Lens (RxLAL) 60005-3205Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)50 reports
- RxSight Light Adjustable Lens (RxLAL) 60005-3200Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)47 reports
- RxSight Light Adjustable Lens (RxLAL) 60005-3210Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)39 reports
- RxSight Light Adjustable Lens (RxLAL) 60005-3190Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)32 reports
- RxSight Light Adjustable Lens (RxLAL) 60005-3195Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)31 reports
- Light Adjustable Lens (LAL) 60007-0200Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)31 reports
- RxSight Light Adjustable Lens (RxLAL) 60005-3215Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)30 reports
- RxSight Light Adjustable Lens (RxLAL) 60005-3185Rxsight, Inc. · Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)29 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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