RecallDepth

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.

Company
Johnson & Johnson Surgical Vision Inc
Recall Initiated
August 6, 2021
Terminated
March 6, 2023
Recall Number
Z-0028-2022
Quantity
1 lens
Firm Location
Santa Ana, CA

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

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

Lot / Code Info

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

Root Cause

Process control

Action Taken

On 08/18/2021, the firm sent via FedEx standard overnight an "URGENT DEVICE Recall" Letter informing customers that it inadvertently release of nonconforming product (high endotoxin levels). Customers are instructed to: 1. Complete and return the Customer Reply Form to acknowledge receipt of the Recall Notice and email to RegCompliOne@its.jnj.com within 3 business days of receipt of the recall notice. 2. Review their patient records to confirm implantation of the impacted lens. 3. If no unexpected postoperative outcome occurred following implantation, no further action is required after Customer Reply Form has been returned. 4. If issues were encountered, inform the Recall Firm by calling 877-266-4543, Option 2. If reporting a complaint, provide the serial number, the date of surgery, a description of the event, and patient outcome. For any questions, contact Customer Support at; 877-266-4543, Option 2 or email RegCompliOne@its.jnj.com

More recalls by Johnson & Johnson Surgical Vision Inc

View all recalls by this company →