Recall
FDAHealthJanuary 7, 2026

Olympus Corporation of the Americas — Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These instruments have been designed to be used with

⚠️ Devices which did not undergo thermoforming could deform and lose performance.

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
January 7, 2026

Worldwide - US Nationwide distribution including in the states of AL, AR, AZ, CA, CO, DC, DE, FL, GA, GU, HI, IA, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, MT, NC, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WA, WI, WV, WY and International: TBD.

What's affected?

Product
Product Name: Single Use 3-Lumen Sphincterotome V Model/Catalog Number: KD-V411M-1520 Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.
Lot code
with

Additional details

Model/Catalog Number: KD-V411M-1520; Material REF: (1) N5411630, (2) N1089910; UDI-DI: (1)04953170380600, (2) N/A; All Lots with a valid expiration date

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 3954 units (OUS only).

View original FDA notice →

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