FDA recall record

Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm recall — FDA Z-3216-2026

Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm,

Class IIclassification
Z-3216-2026official record ID
Sep 30, 2026report date

Recall record at a glance

Official recordZ-3216-2026
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusOngoing
Recalling firmOlympus Corporation of the Americas
Report dateSep 30, 2026
Recall initiation dateAug 19, 2026
Quantity305 units
LocationCenter Valley, PA, United States

Official product description

Olympus EZDilate Endoscopic Balloon Dilator Wired-guided 11, 12, 13mm. Model Number: BD-420X-1355.

Why the product was recalled

Potential for the inflation chart label affixed to the shaft of the device to be incorrect and indicate a balloon diameter of 18, 19, or 20 mm,

Distribution information

International distribution in the country of Japan.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: E-Mail.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

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