Light Adjustable Lens (LAL)Recalls & reported problems across all models
Rxsight, Inc. · 33 models in the FDA device registry
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 341
- Deaths reported
- 0
- Injuries reported
- 341
- Recalls
- 0
We found 33 models of Light Adjustable Lens (LAL) by Rxsight, Inc. in the FDA's device registry (GUDID). Together they are named in 341 adverse event reports in the FDA's MAUDE database, received between Mar 12, 2024 and Sep 30, 2026 — classified as 341 injuries.
The most frequently reported specific device problem is “Optical Decentration” (21 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event. Widely used products collect more reports, so totals can't be used to compare products or estimate failure rates. Only reports that name a model's exact device identifier are counted. What reports can and can't tell you · How this data works
Reports received per month, all models
Most reported Light Adjustable Lens (LAL) problems
Device problems
- Adverse Event Without Identified Device or Use Problem283
- Optical Decentration21
- Use of Device Problem21
- Patient-Device Incompatibility8
- Insufficient Device Problem Information4
- Optical Problem3
- Device Dislodged or Dislocated2
- Detachment of Device or Device Component1
Patient problems
- Blurred Vision165
- Visual Disturbances103
- Unspecified Eye / Vision Problem41
- Capsular Bag Tear32
- Visual Impairment25
- Diplopia/Double Vision20
- Insufficient Information3
- No Clinical Signs, Symptoms or Conditions3
Light Adjustable Lens (LAL) models
33 models, most reported first. Each model has its own page with its reports, recalls and device details.
- Light Adjustable Lens (LAL) 60007-0200Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)31 reports
- Light Adjustable Lens (LAL) 60007-0195Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)29 reports
- Light Adjustable Lens (LAL) 60007-0220Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)27 reports
- Light Adjustable Lens (LAL) 60007-0205Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)26 reports
- Light Adjustable Lens (LAL) 60007-0225Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)25 reports
- Light Adjustable Lens (LAL) 60007-0210Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)24 reports
- Light Adjustable Lens (LAL) 60007-0185Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)21 reports
- Light Adjustable Lens (LAL) 60007-0215Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)18 reports
- Light Adjustable Lens (LAL) 60007-0235Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)16 reports
- Light Adjustable Lens (LAL) 60007-0190Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)15 reports
- Light Adjustable Lens (LAL) 60007-0240Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)14 reports
- Light Adjustable Lens (LAL) 60007-0170Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)11 reports
- Light Adjustable Lens (LAL) 60007-0175Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)11 reports
- Light Adjustable Lens (LAL) 60007-0230Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)11 reports
- Light Adjustable Lens (LAL) 60007-0150Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)8 reports
- Light Adjustable Lens (LAL) 60007-0165Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)7 reports
- Light Adjustable Lens (LAL) 60007-0180Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)7 reports
- Light Adjustable Lens (LAL) 60007-0250Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)7 reports
- Light Adjustable Lens (LAL) 60007-0140Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)5 reports
- Light Adjustable Lens (LAL) 60007-0260Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)5 reports
- Light Adjustable Lens (LAL) 60007-0160Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)4 reports
- Light Adjustable Lens (LAL) 60007-0050Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)3 reports
- Light Adjustable Lens (LAL) 60007-0090Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)3 reports
- Light Adjustable Lens (LAL) 60007-0100Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)2 reports
- Light Adjustable Lens (LAL) 60007-0110Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)2 reports
- Light Adjustable Lens (LAL) 60007-0120Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)2 reports
- Light Adjustable Lens (LAL) 60007-0070Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)1 report
- Light Adjustable Lens (LAL) 60007-0080Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)1 report
- Light Adjustable Lens (LAL) 60007-0130Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)1 report
- Light Adjustable Lens (LAL) 60007-0000Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)1 report
- Light Adjustable Lens (LAL) 60007-0270Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)1 report
- Light Adjustable Lens (LAL) 60007-0290Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)1 report
- Light Adjustable Lens (LAL) 60007-0300Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)1 report
Recent Light Adjustable Lens (LAL) adverse event reports
The 15 most recent reports across all models, in the reporter's own words as published by the FDA.
InjurySep 30, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Blurred Vision
MAUDE report 50948497 ↗InjurySep 28, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Blurred Vision; Visual Disturbances
MAUDE report 50916565 ↗InjurySep 28, 2026Use of Device Problem; Optical Problem
A site reported to RxSight that a patient's Light Adjustable Lens+ (LAL+) was explanted from the left eye (OS) due to blurred vision and changes in manifest refraction (MR) secondary to suspected photopolymerization. The patient had completed two light treatments an no lock-in treatments before presenting to clinic one year later, complaining of blurry vision OS. Slit lamp examination revealed a small central bulge on the LAL+. Additionally, the patient reported not wearing RxSight UV protective eyewear while swimming. The LAL+ was explanted and replaced with another LAL+ without complications.
Patient problems: Blurred Vision
MAUDE report 50915980 ↗InjurySep 25, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Visual Disturbances
MAUDE report 50905982 ↗InjurySep 19, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Blurred Vision
MAUDE report 50831676 ↗InjurySep 17, 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 left eye due to the patient's dissatisfaction with their near vision. No additional information has been provided.
Patient problems: Unspecified Eye / Vision Problem
MAUDE report 50807901 ↗InjurySep 16, 2026Adverse Event Without Identified Device or Use Problem
A site reported to RxSight that a patient's Light Adjustable Lens+ was explanted from the left eye after completion of light treatments due to dissatisfaction with near vision and a new Light Adjustable Lens implanted as a replacement.
Patient problems: Unspecified Eye / Vision Problem
MAUDE report 50790250 ↗InjuryAug 14, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Visual Disturbances
MAUDE report 50262375 ↗InjuryAug 11, 2026Adverse Event Without Identified Device or Use Problem
A site reported to RxSight that a bilaterally implanted patient's Light Adjustable Lens was explanted from the left eye due to blurry vision and difficulty adapting to blended vision after 3 light adjustments.
Patient problems: Blurred Vision
MAUDE report 50212625 ↗InjuryAug 11, 2026Adverse Event Without Identified Device or Use Problem
A site reported to RxSight that a patient's Light Adjustable Lens+ (LAL+) was explanted due to blurry vision, difficulty judging distances and a change in refraction, diagnosed approximately 8 months after completion of light treatments. A new LAL+ was implanted as a replacement.
Patient problems: Blurred Vision; Visual Impairment
MAUDE report 50212623 ↗InjuryAug 11, 2026Insufficient Device Problem Information
A site reported to RxSight that a patient's Light Adjustable Lens+ (LAL+) was explanted and a vitrectomy was performed. No additional information has been provided.
Patient problems: Insufficient Information
MAUDE report 50210962 ↗InjuryAug 6, 2026Optical Decentration
A site reported to RxSight that a bilaterally implanted patient underwent explantation of the Light Adjustable Lens+ (LAL+) in the right eye after two adjustments due to a decrease in visual acuity. Following the first adjustment, the lens was observed to be slightly decentered. The patient was reported to be doing well post-explant. No additional information is available.
Patient problems: Visual Impairment
MAUDE report 50159646 ↗InjuryAug 4, 2026Adverse Event Without Identified Device or Use Problem
A site reported to RxSight that a patient's Light Adjustable Lens+ was explanted from the right eye due to dissatisfaction with the refractive target and the patient's complaint of halos and "smudgy" visual acuity. A Light Adjustable Lens was implanted as a replacement. No additional information was provided.
Patient problems: Visual Disturbances
MAUDE report 50130584 ↗InjuryJul 27, 2026Adverse Event Without Identified Device or Use Problem
A site reported to RxSight that a patient's Light Adjustable Lens+ was explanted due to the patient's dissatisfaction with distance and intermediate vision after completion of light treatments and a new Light Adjustable Lens implanted as a replacement. No additional information is available.
Patient problems: Unspecified Eye / Vision Problem
MAUDE report 50018961 ↗InjuryJul 27, 2026Insufficient Device Problem Information
A site reported to RxSight that a patient's Light Adjustable Lens+ was explanted due to being implanted backwards during the initial implantation surgery. A new LAL+ was implanted successfully as a replacement with no complications.
Patient problems: Unspecified Eye / Vision Problem
MAUDE report 50010775 ↗
Other Rxsight, Inc. products
All Rxsight, Inc. devices →Sources and updates
- Models: FDA GUDID, file dated Oct 13, 2026. Models are grouped by the brand name the manufacturer registered.
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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