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Recall Observatory FDA recall evidence

Device product

TECNIS Eyhance IOL, REF: ICB00, STERILE.EO, Rx Only

Z-2289-2023

July 06, 2023

Class II

Product summary

Firm
Johnson & Johnson Surgical Vision, Inc.
Event
Event 92666
Status
Ongoing
Classification
Class II
Quantity
61 units
Official record key
device-enforcement:Z-2289-2023

Official wording

Reason: Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.

Code information: UDI-DI: N/A/ Serial Numbers: 8046642236, 8046652236, 8046662236, 8046672236, 8046682236, 8046692236, 8046702236, 8046712236, 8046722236, 8046732236, 8046742236, 8046752236, 8046762236, 8046772236, 8046782236, 8046792236, 8046802236, 8046812236, 8046822236, 8046832236, 8046842236, 8046852236, 8046862236, 8046872236, 8046882236, 8046892236, 8046902236, 8046912236, 8046922236, 8046932236, 8046942236, 8046952236, 8046962236, 8046972236, 8046982236, 8046992236, 8047002236, 8047012236, 8047022236, 8047032236, 8047042236, 8047052236, 8047062236, 8047072236, 8047082236, 8047102236, 8047112236, 8047122236, 8047132236, 8047142236, 8047152236, 8047162236, 8047172236, 8047182236, 8047192236, 8047202236, 8047212236, 8047222236, 8047232236, 8047242236, 8047252236

Distribution pattern: International distribution to the countries of China, India, Korea.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Their is a potential that intraocular lenses (IOLs) were manufactured with unintended toric fiducial marks.