Skip to content
Recall Observatory FDA recall evidence

Device product

TECNIS Eyhance IOLs are permanent intraocular implants intended for implantation in the capsular bag. The TECNIS Simplicity Delivery System is designed as a single-use disposable preloaded modular cartridge that functions as both the primary packaging and as a sterile, disposable insertion system for delivering the IOL into the eye during cataract surgery.

Z-0028-2022

August 06, 2021

Class II

Product summary

Firm
Johnson & Johnson Surgical Vision Inc
Event
Event 88564
Status
Terminated
Classification
Class II
Quantity
1 lens
Official record key
device-enforcement:Z-0028-2022

Official wording

Reason: Nonconforming product was distributed in error. Product was nonconforming due endotoxin levels higher than both the Firm's internal endotoxin specification limit and the FDA recommended endotoxin specification limit. Product was released in error based on the results of additional testing performed during the investigation into release testing nonconformance.

Code information: Model: DIU225U050 UDI Code: (01)05050474745831(17)240414(21)5248142104 Production Order Number: 900001985625 Serial Number: 5248142104

Distribution pattern: U.S. Nationwide distribution in the state of IL.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    Nonconforming product was distributed in error. Product was nonconforming due endotoxin levels higher than both the Firm's internal endotoxin specification limit and the FDA recommended endotoxin specification limit. Product was released in error based on the results of additional testing performed during the investigation into release testing nonconformance.