FDA Enforcement Class II Ongoing

EZDilate Wire Guided Balloon- Indicated for use in adult and adolescent (> 12 years) populations to endoscopically dilate strictures of the alimentary tract. It is also indicated in adults for endoscopic dilatation of the Sphincter of Oddi with or without prior sphincterotomy. Model/Catalog Number: BD-410X-1055

Recall: Z-0225-2025 · Reported October 30, 2024

Enforcement

Recall Number
Z-0225-2025
Event ID
95400
Classification
Class II
Status
Ongoing
Product Type
Devices
Firm
Olympus Corporation of the Americas
Voluntary / Mandated
Voluntary: Firm initiated
Initial Notification
Letter
Report Date
October 30, 2024
Initiation Date
September 13, 2024
Classification Date
October 24, 2024
Address
3500 Corporate Pkwy, N/A, Center Valley, PA, 18034-8229, United States

Description

EZDilate Wire Guided Balloon- Indicated for use in adult and adolescent (> 12 years) populations to endoscopically dilate strictures of the alimentary tract. It is also indicated in adults for endoscopic dilatation of the Sphincter of Oddi with or without prior sphincterotomy. Model/Catalog Number: BD-410X-1055

Reason

Mislabeled Glo Cath Label (attached to the device) states: 11 mm, 12 mm, 13 mm however the balloon is 8.5mm, 9.5mm and 10.5 mm and may result in prolonged surgery. All other labeling is correct for the balloon, including the Shelf Box with Front Box Label and Circular Star Label and the balloon Pouch

Code Info

UDI-DI: 821925033238 Lot: 408987

Distribution

Worldwide Distribution: US distribution to states of: CA, FL, IL, NJ, NY, PA, TN, VA, WI; and Foreign OUS to countries of: CA, DE, IN, SG, Latin America.

Quantity

209 units