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Recall Observatory FDA recall evidence

Device product

EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for endoscopic dilation of strictures of the esophagus in adults and adolescents (>12 years). Model: BD-400P-1580

Z-0936-2024

November 10, 2023

Class II

Product summary

Firm
Olympus Corporation of the Americas
Event
Event 93508
Status
Ongoing
Classification
Class II
Quantity
5232 units
Official record key
device-enforcement:Z-0936-2024

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: 360910, 360911, 364014, 364158, 364338, 367646, 367647, 367648, 383363, 383846, 383847, 384058

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