Katalyst Surgical recalls specific DEX Ophthalmic Tissue Forceps models due to a field safety issue requiring corrective action per IFU. Affected units have unique model and lot numbers listed in the recall notice.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Katalyst Surgical is recalling certain DEX Ophthalmic Tissue Forceps models because of a safety issue that requires corrective action as per the manufacturer's instructions. This recall affects specific lot numbers and model numbers with expiration dates up to November 2028.
The recall mentions a field safety corrective action for the product's instructions, but the specific hazard mechanism is not clearly described in the notice. Without details on how the issue could cause harm, the risk level cannot be determined.
Medical professionals using these surgical forceps are likely affected. Patients undergoing procedures with these instruments may be at risk if the recall is not addressed.
Check for the model number DVF4022-25-S on the forceps. Affected units have specific lot numbers (M50093 through M50997) and expiration dates from August 2028 to November 2028.
Look for the model number DVF4022-25-S and lot numbers M50093 to M50997 on the forceps.
The recall mentions a field safety corrective action for the product's instructions, but the specific hazard mechanism is not clearly described in the notice.
Check for the model number DVF4022-25-S and lot numbers M50093 through M50997 on the forceps.
The recall does not specify a remedy or immediate action, so there is no instruction to stop using them now.
We’ve drafted a message you can send Katalyst Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2077-2026 — Katalyst Surgical Katalyst Surgical Hello, I own a Katalyst Surgical that is covered by recall Z-2077-2026 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.
