Katalyst Surgical recalls DEX Ophthalmic Tissue Forceps model DVF4034-25-S due to field safety corrective action. Affected units have specific lot numbers and expiration dates.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Katalyst Surgical is recalling DEX Ophthalmic Tissue Forceps with model number DVF4034-25-S. This recall is due to a field safety corrective action required by the manufacturer to address potential safety issues.
The recall involves a field safety corrective action for the DEX Forceps and Scissors. This indicates a potential safety issue that requires correction to prevent harm during medical procedures.
Medical professionals using these surgical instruments are likely affected. Patients undergoing procedures with these instruments may be at risk if the recall is not addressed.
Check for model number DVF4034-25-S on the product. Affected units have specific lot numbers (M47337, M50921, M51525, M51526, M52172) and expiration dates (up to 02/20/2029).
Identify the model number and lot numbers to confirm if your DEX Ophthalmic Tissue Forceps are affected.
The model number is DVF4034-25-S.
Affected lot numbers include M47337, M50921, M51525, M51526, and M52172.
The expiration dates range from 04/29/2028 to 02/20/2029.
We’ve drafted a message you can send Katalyst Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2079-2026 — Katalyst Surgical Katalyst Surgical Hello, I own a Katalyst Surgical that is covered by recall Z-2079-2026 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.
