medical Class II Updated 2024-10-30

Olympus Corporation of the Americas recalls EZDilate Wire Guided Balloon- Indicated for use in adult and

Recalled Product

EZDilate Wire Guided Balloon- Indicated for use in adult and adolescent (> 12 years) populations to endoscopically dilate strictures of the alimentary tract. It is also indicated in adults for endoscopic dilatation of the Sphincter of Oddi with or without prior sphincterotomy. Model/Catalog Number: BD-410X-1055


Hazard / Issue

Mislabeled Glo Cath Label (attached to the device) states: 11 mm, 12 mm, 13 mm however the balloon is 8.5mm, 9.5mm and 10.5 mm and may result in prolonged surgery. All other labeling is correct for the balloon, including the Shelf Box with Front Box Label and Circular Star Label and the balloon Pouch

Issued by

FDA

Affected States: CA, FL, IL, NJ, NY, PA, TN, VA, WI, DE, IN
Lot/Code Info: UDI-DI: 821925033238 Lot: 408987
View official government recall

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