PREVUE C PREVUE (clear), +15.50DRecalls & reported problems
Hoya Medical Singapore Pte. Ltd. · Foldable, posterior chamber intraocular lens (IOL), preloaded in an injector that automatically folds the lens as it is advanced, prior to insertion. Single use. · Class 3 · Implant
All models of PREVUE C (14)
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 10757770564061), received between Jun 30, 2022 and Jun 5, 2023 — classified as 2 injuries.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (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
- Material Split, Cut or Torn1
- Sharp Edges1
Patient problems
- Failure of Implant2
- Capsular Bag Tear1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryJun 5, 2023Sharp Edges; Sharp Edges
INTRA-OPERATIVE COMPLICATIONS. CAPSULE RUPTURE, EXPLANTATION WHILE INSERTING THE LENS, IT TORE THE CAPSULE. NO INCISION ENLARGEMENT; PRODUCT REPLACED WITH ANOTHER LENS IMMEDIATELY DURING SURGERY. NO PERMANENT OR NEGATIVE IMPACT ON PATIENT HEALTH EXPECTED.
Patient problems: Capsular Bag Tear; Failure of Implant
MAUDE report 17067451 ↗InjuryJun 30, 2022Material Split, Cut or Torn; Material Split, Cut or Torn
DAMAGED HAPTIC AFTER IMPLANTATION. IT WAS REPORTED THAT THE HAPTIC BROKE AND CAUSED A VITRECTOMY; LENS REPLACED IMMEDIATELY DURING SURGERY. PATIENT IMPACT: EXPLANTATION.
Patient problems: Failure of Implant
MAUDE report 14881286 ↗
Other Intraocular Lens devices
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- 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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