iSert Intraocular Lens 230 (clear), +19.00DRecalls & reported problems
Hoya Medical Singapore Pte. Ltd. · Class 3 · Implant
All models of iSert Intraocular Lens (69)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 04547480301297), received between Feb 23, 2018 and Jun 30, 2022 — classified as 2 injuries.
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
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
Patient problems
- Eye Injury1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 30, 2022Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
DATE OF IMPLANT: (B)(6) 2021. DATE OF EVENT: (B)(6) 2021. POST-OPERATIVE COMPLICATION; GLISTENING. IT WAS CONFIRMED THAT THERE WAS NO LOSS OF BEST CORRECTED VISUAL ACUITY; NO YAG OR EXPLANT REQUIRED. LENS REMAINS IMPLANTED IN PATIENTS EYE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 14881395 ↗InjuryFeb 23, 2018Adverse Event Without Identified Device or Use Problem
REPORTEDLY, A TEAR IN THE IOL WAS NOTICED AFTER IOL INSERTION INTO THE RIGHT EYE. THE LENS WAS REMOVED AND REPLACED WITH THE BACKUP LNES OF THE SAME MODEL AND THE SAME DIOPTER. THE INCISION WAS ENLARGED TO REMOVE THE LENS. SUTURES WERE PLACED AS A PART OF STANDARD PRCEDURE. PATIENT PROGNOSIS AND OUTCOME ARE GOOD.
Patient problems: Eye Injury
MAUDE report 7293490 ↗
Other Intraocular Lens devices
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens146 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens145 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens144 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens139 reports
- TECNIS SIMPLICITY DIB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens1 recall81 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens129 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens127 reports
- TECNIS IOL PCB00Johnson & Johnson Surgical Vision, Inc. · intraocular lens126 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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