TECNIS CL IOL Z9002 (REF Z900200085)Recalls & reported problems
Johnson & Johnson Surgical Vision, Inc. · TECNIS CL MONO 13MM 8.5 · Class 3 · Implant
All models of TECNIS CL IOL (42)
Data updated Oct 16, 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 05050474530461), received between Oct 9, 2020 and Oct 9, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Unintended Movement” (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
Device problems
- Unintended Movement1
Patient problems
- Blurred Vision1
- Visual Disturbances1
- Vitrectomy1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 9, 2020Unintended Movement; Unintended Movement
IT WAS REPORTED THAT THE INTRAOCULAR LENS (IOL) WAS DISLOCATED IN THE PATIENT'S LEFT EYE AS THE PATIENT HAD POOR BAG SUPPORT. THE PATIENT COMPLAINED OF BLURRINESS AND CLOUDY VISION FOR 5 MONTHS. THE IOL WAS REPOSITIONED, WITH SCLERAL FIXATION, AND A PARS PLANA VITRECTOMY WAS REQUIRED. THROUGH FOLLOW-UP IT WAS CONFIRMED THAT THE PATIENT IS DOING WELL POST REPOSITIONING. THE PATIENT'S LAST VISIT WAS ON (B)(6) 2020, THE IOL WAS CENTERED, UNCORRECTED VISION WAS 20/50, AND THE PATIENT PIN HOLED TO 20/30. NO ADDITIONAL INFORMATION WAS PROVIDED.
Patient problems: Blurred Vision; Visual Disturbances; Vitrectomy
MAUDE report 10654118 ↗
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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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