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Recall Observatory FDA recall evidence

Device product

EZDilate Wire Guided Balloon 11-12-13. Indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years). Model: BD-410X-1355

Z-0941-2024

November 10, 2023

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 93508
Status
Ongoing
Classification
Class II
Quantity
3354 units
Official record key
device-enforcement:Z-0941-2024

Official wording

Reason: Product balloon issues: inflating, deflating and/or retrieving the devices; reports of bursting and leaking and events involving foreign body in patient and prolonged procedure.

Code information: UDI-DI: 00821925033245 Lot Numbers: 369715, 370108, 370270, 370496, 377814, 378933, 379534, 386461, 386462, 388459

Distribution pattern: Nationwide. Foreign: AU BR BR CA DE HK IN JP SG

Derived failure modes

  • Foreign material or chemical contamination

    reason.foreign_material_chemical_contamination · v1.0.0

    foreign body