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.
Action Details
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
Distribution Pattern
U.S. Nationwide distribution in the state of IL.
Code Information / Serial Numbers
Model: DIU225U050
UDI Code: (01)05050474745831(17)240414(21)5248142104
Production Order Number: 900001985625
Serial Number: 5248142104
Public Record Disclaimer
This page represents an index of public-record FDA device recalls. It does not imply current safety or compliance status of the product. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Refer to official government sources for primary safety alerts.