medical Class II Updated 2024-02-07

Olympus Corporation of the Americas recalls EZDilate Fixed Wire Balloon 13.5-14.5-15.5. Indicated for en

Recalled 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


Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI-DI: 00821925033191 Lot Numbers: 360910, 360911, 364014, 364158, 364338, 367646, 367647, 367648, 383363, 383846, 383847, 384058
View official government recall

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