Katalyst Surgical recalls DEX Ophthalmic Tissue Forceps (Model DVF4019-25-S) due to field safety corrective action. Check product details to determine if your item is affected.
Field Safety Corrective Action for IFU in DEX Forceps and Scissors.
Katalyst Surgical is recalling specific models of DEX Ophthalmic Tissue Forceps that have a field safety issue. This recall requires checking your product details to see if it's affected, but no immediate action is needed beyond verifying the model.
The recall involves a field safety corrective action for the DEX Forceps and Scissors. This means there's a potential issue with the product that could affect safety during medical procedures, but the exact hazard isn't specified in the notice.
Medical professionals who use these surgical instruments are most likely affected. Patients using these tools during procedures may be at risk if the instruments are defective.
Check for the model number DVF4019-25-S on the product. The lot numbers and expiration dates listed in the recall details indicate specific batches that are affected.
Verify your DEX Ophthalmic Tissue Forceps model number and lot number to see if it matches the recalled items listed in the notice.
The recall is for a field safety corrective action, but the specific hazard isn't detailed in the notice.
No immediate action is required beyond checking if your product matches the recalled details.
Check for the model number DVF4019-25-S and the specific lot numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send Katalyst Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-2075-2026 — Katalyst Surgical Katalyst Surgical Hello, I own a Katalyst Surgical that is covered by recall Z-2075-2026 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.
