Light Adjustable Lens (LAL) 60007-0300Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00818806021729), received between Jun 3, 2026 and Jun 3, 2026 — classified as 1 injury.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (1 report).

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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryJun 3, 2026Detachment of Device or Device Component

  A SITE REPORTED TO RXSIGHT THAT THE TRAILING HAPTIC WAS DISINSERTED DURING A LIGHT ADJUSTABLE LENS+ (LAL+) IMPLANTATION. THE LAL+ WAS REMOVED DURING THE SAME SURGERY AND THE PATIENT WAS LEFT APHAKIC. A SECONDARY SURGICAL PROCEDURE WAS SUCCESFULLY COMPLETED THE FOLLOWING DAY TO IMPLANT ANOTHER LAL. NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 25374671 ↗