MST ArcDUO Ophthalmic Knife (MicroSurgical) – Contamination Risk (2025)
Contaminated springs in a suction set may potentially cause minor eye irritation.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
MST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48-1000-01
Brand
MicroSurgical Technology Inc
Lot Codes / Batch Numbers
UDI:00844685014316. Lots: 207552 and 208238
Products Sold
UDI:00844685014316. Lots: 207552 and 208238
MicroSurgical Technology Inc is recalling MST ArcDUO 9mm, REF: ARC-0002, single-use, sterile ophthalmic knife, used with Suction Set, Part: 48 due to An ophthalmic knife has a suction set (not direct patient-contacting), which contains springs contaminated with an unidentified residue that may poten. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
On 8/20/2025, a recall notice was sent to a surgery center that was asked to return the affected devices and provide information on affected device disposition. The customer was also asked, if they further distributed affected devices, to notify their customers of the recall For additional information, contact the firm at MSTcomplaints@microsurgical.com
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026