D.O.R.C. recalls TDC VELOCE 25G Two Dimensional Cutters with loose outer knife that may become loose during use. Affected models include Article Numbers 9268.VIT25 and others listed. Stop using if you have these items.
An increase in incidence in complaints of a loose outer knife and reports of the outer knife becoming loose during use.
D.O.R.C. is recalling TDC VELOCE 25G Two Dimensional Cutters because the outer knife can become loose during use. This poses a risk of injury if the knife slips while cutting.
The outer knife can become loose during normal use, which may cause it to slip and potentially injure the user. This is a mechanical issue that affects the device's stability and safety.
Users of the TDC VELOCE 25G Two Dimensional Cutter for medical procedures are most at risk. This includes healthcare professionals who use the device for eye treatments.
Check for Article Numbers: 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, or other listed numbers. The device was sold with specific lot numbers and UDI-DI codes.
Look for the Article Number on the device or its packaging to confirm if it's affected.
If the outer knife feels loose, stop using the device immediately to prevent injury.
The recall is due to reports of the outer knife becoming loose during use, which could lead to injury if the knife slips.
Affected models include Article Numbers 9268.VIT25, 9311.25G01, 9311.25G02, 9311.25K01, and others listed in the recall notice.
The recall does not specify a return process, so contact D.O.R.C. directly for guidance if you have an affected device.
We’ve drafted a message you can send D.O.R.C. to request your refund or repair — edit it as you like.
Subject: Recall Z-2323-2026 — D.O.R.C. D.O.R.C. Hello, I own a D.O.R.C. that is covered by recall Z-2323-2026 from D.O.R.C.. 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.
