TECNIS SIMPLICITY recallZ-1634-2026 · AMO Puerto Rico Manufacturing, Inc. · initiated Feb 19, 2026

Why it was recalled

Due to identifying a limited quantity of intraocular lenses that may have a haptic that sticks to the optic which prevents the lens from unfolding as consistently as expected.

FDA root cause category: Process control

What the company is doing

On 02/19/2026, the firm send via FedEx an "URGENT: MEDICAL DEVICE RECALL" Letter to customers informing them that in a limited quantity of TECNIS Eyhance IOL (intraocular lens) with TECNIS Simplicity" Delivery System (DIB00) products exhibit an occurrence of haptics sticking to the optic, which can prevent the lens from unfolding as expected following lens insertion during the surgical procedure. Customers are instructed to: 1. Identify if any inventory contains TECNIS Eyhance IOL (intraocular lens) with TECNIS Simplicity" Delivery System (DIB00). 2. Do not use and remove all affected TECNIS Eyhance IOL (intraocular lens) with TECNIS Simplicity" Delivery System (DIB00) from inventory. 3. Complete Customer Reply Form. It is required information for reconciliation purposes with regulatory agencies, even if you have no inventory. For products to be returned: " Complete the Customer Reply Form, noting the serial number of the TECNIS Eyhance IOL (intraocular lens) with TECNIS Simplicity" Delivery System (DIB00). " Use the provided return label or contact the Global Post Market Safety Team at 1-877-266-4543, Option 2 to obtain an RGA number and arrange product return. " Email Customer Reply Form to [email protected] within 3 business days of receipt of this letter. " If issues were encountered, inform JJSV by calling the Global Post Market Safety Team 1-877-266-4543, Option 2 or send an email to [email protected] . If reporting a complaint, provide the serial number, the date of surgery, a description of the event, and patient outcome. " Return affected product as soon as possible. The firm will work directly with customers to replace the affected unit and provide any necessary next steps. If you do not have product to be returned: " Review your patient records to confirm implantation of the impacted lens. No further action is required after the Customer Reply Form has been returned.

Recall details

Recall number

Z-1634-2026

Status

Open, Classified

Initiated by the company

Feb 19, 2026

Posted by the FDA

Mar 24, 2026

Recalling firm

AMO Puerto Rico Manufacturing, Inc.

Quantity

361

Product code

HQL

FDA submissions

P980040, P980040S117

Distribution

U.S Nationwide distribution in the states of CA,FL, IL, ME,MS, NJ, NY, OK, OR, TX, and WI.

Product description

Brand Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Product Name: TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System Model/Catalog Number: DIB00 Software Version: N/A Product Description: The TECNIS SIMPLICITY" Delivery System is designed to provide a sterile,controlled and touch-free method of delivering the lens into the eye. The lens is preloaded and pre-assembled in the delivery system. The TECNIS SIMPLICITY" Delivery System Model DIB00 contains the TECNISEyhance" IOL, which is a one-piece, foldable, posterior chamber lens with an overall diameter of 13.0 mm and an optic diameter of 6.0 mm. The TECNIS SIMPLICITY" Delivery System is designed to provide a sterile,controlled and touch-free method of delivering the lens into the eye. Component: No

Devices named in this recall

1 device in the FDA device registry whose identifier appears in the recall's code information.

• TECNIS SIMPLICITY DIB00

  Johnson & Johnson Surgical Vision, Inc. · intraocular lens
  1 recall81 reports

Product lines

• TECNIS SIMPLICITYJohnson & Johnson Surgical Vision, Inc. · 112 models · 2,730 reports · 1 recall