medical Class II Updated 2024-02-07

Olympus Corporation of the Americas recalls EZDilate Wire Guided Balloon 8.5-9.5-10.5. indicated for end

Recalled 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


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