MicroSurgical Technology recalls ArcDUO 9mm ophthalmic knives with contaminated suction sets that may cause eye irritation. Affected units include specific lots and part numbers.
An ophthalmic knife has a suction set (not direct patient-contacting), which contains springs contaminated with an unidentified residue that may potentially cause eye irritation
MicroSurgical Technology is recalling ArcDUO 9mm ophthalmic knives that come with suction sets containing potentially contaminated springs. This could cause eye irritation if used improperly.
The suction set contains springs contaminated with an unidentified residue that may cause eye irritation when used during eye surgery. This is a potential risk if the contaminated residue comes into contact with the eye.
Ophthalmic surgeons and medical professionals who use the ArcDUO 9mm knives with suction sets. Those using the specific lots (207552 and 208238) and part number 48-1000-01 are most at risk.
Check for the product name 'ArcDUO 9mm', reference number ARC-0002, part number 48-1000-01, and lots 207552 or 208238. The unique device identifier (UDI) is 00844685014316.
Identify the product name, reference number, part number, and lot numbers to confirm if your item is affected.
The recall states the suction set may cause eye irritation, but it does not mention serious injury or death. This is a low-risk hazard.
The recall does not specify a remedy, so you should check the product details to see if it is affected. If it is, contact MicroSurgical Technology for further instructions.
Look for the product name 'ArcDUO 9mm', reference number ARC-0002, part number 48-1000-01, and lots 207552 or 208238.
We’ve drafted a message you can send MicroSurgical Technology to request your refund or repair — edit it as you like.
Subject: Recall Z-0411-2026 — MicroSurgical Technology MicroSurgical Technology Hello, I own a MicroSurgical Technology that is covered by recall Z-0411-2026 from MicroSurgical Technology. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
