Bausch + Lomb BL5323WRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00757770058112), received between Mar 20, 2017 and Mar 20, 2017 — classified as 1 injury.

The most frequently reported specific device problem is “Material Fragmentation” (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 16, 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.

• InjuryMar 20, 2017Material Fragmentation; Material Fragmentation

  THE TROCAR CANNULA BROKE WHILE IN THE EYE. HALF OF THE CANNULA WAS REMOVED FROM THE EYE AND THE OTHER HALF FELL INTO THE VITREOUS. A SECOND PROCEDURE WAS PERFORMED ON (B)(6) 2017 TO REMOVE THE FOREIGN BODY FROM THE EYE. ADDITIONAL INFORMATION RECEIVED STATES THE SURGEON REPROCESSED AND REUSED THE DISPOSABLE PRODUCT.

  Patient problems: Eye Injury

  MAUDE report 6417435 ↗