Trulign® Toric IOL BL1UTRecalls & reported problems
Bausch & Lomb Incorporated · Trulign toric posterior chamber intraocular lens +25.50D SE / +2.75D CYL · Class 3 · Implant
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 10757770521392), received between Sep 8, 2023 and Sep 8, 2023 — classified as 1 injury.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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
Device problems
- Device Dislodged or Dislocated1
Patient problems
- Blurred Vision1
- Capsular Contracture1
- UGH (Uveitis Glaucoma Hyphema) Syndrome1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 8, 2023Device Dislodged or Dislocated; Device Dislodged or Dislocated
IT WAS REPORTED THAT APPROXIMATELY TEN WEEKS AFTER IMPLANTATION AN INTRAOCULAR LENS (IOL) INTO THE LEFT EYE, POSTERIOR AND ASYMMETRIC LENS VAULTING WAS OBSERVED. IT ALSO WAS REPORTED THE PATIENT DEVELOPED UVEITIS GLAUCOMA HYPHEMA (UGH) SYNDROME. THE IOL WAS EXCHANGED WITH A DIFFERENT MODEL DUE TO UNRESOLVED Z-SYNDROME AND CAPSULAR PHIMOSIS WITHIN A WEEK OF ONSET OF SYMPTOMS. YAG CAPSULOTOMY WAS PERFORMED ONE DAY POST IOL EXCHANGE. IN THE EXPLANTING SURGEON''S OPINION, THE LIKELY CAUSE OF THE EVENT IS CAPSULAR CONTRACTION. IN THE IMPLANTING SURGEON''S OPINION, THE MOST LIKELY CAUSE OF THE EVENT IS SIZE OF THE LENS RELATIVE TO THE SULCUS DIAMETER, CAPSULAR FIBROSIS, AND CAPSULAR PHIMOSIS. PATIENT OUTCOME IS GOOD.
Patient problems: Blurred Vision; Capsular Contracture; UGH (Uveitis Glaucoma Hyphema) Syndrome
MAUDE report 17712135 ↗
Other Lens, Intraocular, Toric Optics devices
- TECNIS IOL ZCT150Johnson & Johnson Surgical Vision, Inc. · LENS, INTRAOCULAR, TORIC OPTICS1 recall7 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS43 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS36 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS32 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS30 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS29 reports
- Clareon CNWTT0Alcon Laboratories, Inc. · LENS, INTRAOCULAR, TORIC OPTICS21 reports
- TECNIS IOL DIU150Johnson & Johnson Surgical Vision, Inc. · LENS, INTRAOCULAR, TORIC OPTICS19 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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