Skip to content
Recall Observatory FDA recall evidence

Device product

Product Name: Single Use 3-Lumen Sphincterotome V (Distal Wire guided) Model/Catalog Number: KD-VC433Q-0720; Software Version: N/A Product Description: These instruments have been designed to be used with an Olympus endoscope and guidewire for papillotomy using high-frequency current.

Z-1283-2026

January 07, 2026

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 98252
Status
Ongoing
Classification
Class II
Quantity
1504 units (350 US, 1154 OUS)
Official record key
device-enforcement:Z-1283-2026

Official wording

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

Code information: Model/Catalog Number: KD-VC433Q-0720; Material REF: (1) N5391710, (2) N5391730, (3) N5778030; UDI-DI: (1) 04953170371219, (2) 04953170371219, (3) 04953170371219; All Lots with a valid expiration date

Distribution pattern: 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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

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