Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

Class 2 Device Recall TECNIS Eyhance IOL with TECNIS Simplicity" Delivery System

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back to Search Results
 Class 2 Device Recall TECNIS Eyhance IOL with TECNIS Simplicity" Delivery Systemsee related information
Date Initiated by FirmFebruary 19, 2026
Date PostedMarch 24, 2026
Recall Status1 Open3, Classified
Recall NumberZ-1634-2026
Recall Event ID 98402
PMA NumberP980040 P980040S117 
Product Classification intraocular lens - Product Code HQL
ProductBrand 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
Code Information Lot Code: GTIN: 05050474731776 SKU: DIB00U0210-12 Serial Numbers: 2409342403 2410072403 2409612403 2409692403 2409752403 2891682403 2891132403 2892032403 2531882403 2531902403 2531212403 2530842403 2531242403 2531892403 2531622403
FEI Number 2648035
Recalling Firm/
Manufacturer		 AMO Puerto Rico Manufacturing, Inc.
Rd # 402 North Km 4.2, Industrial Park
Anasco PR 00610
Manufacturer Reason
for Recall		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 Determined
Cause 2		Process control
ActionOn 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 JJV-US-ProductExperience@its.jnj.com 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 JJV-US-ProductExperience@its.jnj.com . 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.
Quantity in Commerce361
DistributionU.S Nationwide distribution in the states of CA,FL, IL, ME,MS, NJ, NY, OK, OR, TX, and WI.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 The manufacturer has initiated the recall and not all products have been corrected or removed. This record will be updated as the status changes.
PMA DatabasePMAs with Product Code = HQL
-
-