Recall Z-2069-2026 ยท HNR Forceps, Ophthalmic
Katalyst Surgical, LLC
DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog Number: DVF4005-23
| Date | May 6, 2026 (initiated Mar 25, 2026) |
| Status | Open, Classified |
| Reason | Field Safety Corrective Action for IFU in DEX Forceps and Scissors. |
| Root cause | Under Investigation by firm |
| Action | A Field Safety Notification: Field Safety Corrective Action for IFU in DEX Forceps and Scissors dated 3/19/26 was sent to customers. FIELD SAFETY ACTIONS REQUIRED As a customer identified in the receipt of one or more of the affected lots, you are requested/required to take the following steps: 1. Please confirm receipt of this Field Safety Notification by email, either by replying to the sender or using the email addresses listed in the signature at the bottom of this notice. 2. Review the Individualized List of Affected Lot Numbers by Customer provided in the email for lots that were dist |
| Quantity | 5 units |
| Distribution | Worldwide distribution - US Nationwide and the countries of Peru, Argentina, South Korea, Japan, France. |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
This recall record lists no 510(k) number.