Skip to content
Recall Observatory FDA recall evidence

Device product

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

Z-0225-2025

September 13, 2024

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 95400
Status
Ongoing
Classification
Class II
Quantity
209 units
Official record key
device-enforcement:Z-0225-2025

Official wording

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 information: UDI-DI: 821925033238 Lot: 408987

Distribution pattern: 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.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Mislabeled