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Recall Observatory FDA recall evidence

Device product

EZDilate Fixed Wire Balloon 16-17-18. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). Model: BD-400P-1880

Z-0937-2024

November 10, 2023

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 93508
Status
Ongoing
Classification
Class II
Quantity
5031 units
Official record key
device-enforcement:Z-0937-2024

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: 00821925033191 Lot Numbers: 365375, 365823, 365824, 365825, 369028, 382273, 382350, 382351, 383160 Added 12/1/23: 376575, 376888,376914

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