Z-0028-2022 Class II Terminated

Recalled by Johnson & Johnson Surgical Vision Inc — Santa Ana, CA

Recall Details

Product Type
Devices
Report Date
October 13, 2021
Initiation Date
August 6, 2021
Termination Date
March 6, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1 lens

Product Description

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.

Reason for Recall

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.

Distribution Pattern

U.S. Nationwide distribution in the state of IL.

Code Information

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