FDA recall record

Numed BIB Balloon in Balloon Dilatation Catheter recall — FDA Z-1754-2025

Balloon extension lumens are not printed correctly. Specifically, the inner balloon inflation hub was labeled as the outer balloon, and the outer balloon…

Class IIclassification
Z-1754-2025official record ID
May 21, 2025report date

Recall record at a glance

Official recordZ-1754-2025
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusTerminated
Recalling firmNumed Inc.
Report dateMay 21, 2025
Recall initiation dateApr 21, 2025
Quantity4 units
LocationHopkinton, NY, United States

Official product description

BIB Balloon in Balloon Dilatation Catheter. Model Number: 420

Why the product was recalled

Balloon extension lumens are not printed correctly. Specifically, the inner balloon inflation hub was labeled as the outer balloon, and the outer balloon inflation hub was labeled as the inner balloon.

Distribution information

US distribution to Pennsylvania.

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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