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Recall Observatory FDA recall evidence

Device product

EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for endoscopic dilation of strictures in the alimentary tract in adults and adolescents (>12 years) Model: BD-410X-1055

Z-0940-2024

November 10, 2023

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 93508
Status
Ongoing
Classification
Class II
Quantity
2991 units
Official record key
device-enforcement:Z-0940-2024

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:00821925033238 Lot Numbers: 361663, 361664, 365174, 374533, 374534, 375148, 378070, 386123, 386124, 386395

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