Katalyst Surgical recalls DEX Ophthalmic Tissue Forceps (Model DVF4005-25) due to field safety corrective action. Affected units have specific lot numbers and expiration dates. Consumers should contact the manufacturer for details.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Katalyst Surgical is recalling DEX Ophthalmic Tissue Forceps with model number DVF4005-25 because of a field safety issue. This recall affects medical devices used in eye surgery procedures. The hazard requires immediate attention to prevent potential safety risks during use.
The recall is for a field safety corrective action, but the specific hazard mechanism is not clearly described in the record. The manufacturer has issued a correction to the instructions for use to address potential safety concerns.
Medical professionals who use DEX Ophthalmic Tissue Forceps for eye surgery procedures are most at risk. Patients undergoing eye surgery with these specific forceps may also be affected.
Check for the model number DVF4005-25 on the forceps. Affected units have lot number M50530 and expire by September 24, 2028.
Reach out to Katalyst Surgical for specific instructions on how to handle the recalled forceps.
The recall is for a field safety corrective action as stated in the manufacturer's instructions for use. The specific hazard mechanism is not clearly described in the record.
Contact Katalyst Surgical directly for details on how to handle the recalled forceps.
The record mentions a field safety corrective action but does not specify the exact hazard or risk level.
We’ve drafted a message you can send Katalyst Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2070-2026 — Katalyst Surgical Katalyst Surgical Hello, I own a Katalyst Surgical that is covered by recall Z-2070-2026 from Katalyst Surgical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
