Recall
FDAHealthMarch 18, 2026

Diversatek Healthcare — Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 15mm-16.5mm-18mm, REF 1205-18

⚠️ The catheter inflation tag attached to the device may contain an incorrect part number with incorrect balloon diameter sizes and inflation pressures for each stage.

Is this relevant to me?

Geography
US, MO, CA, FL, TX, AZ, PA, RI, NC, IL, MS, KS, NY, OH, VA, LA, IA, MI, NJ, AL
Source agency
FDA
Category
Health
Published
March 18, 2026

US: MO, CA, FL, TX, AZ, PA, RI, NC, IL, MS, KS, NY, OH, VA, LA, IA, MI, NJ, AL, Brazil, Belgium

What's affected?

Product
Diversatek Healthcare Viper¿ 3-Stage Wire Guided Balloon Dilator, 15mm-16.5mm-18mm, REF 1205-18
Lot code
005985

Additional details

UDI/DI 00816734021798, Lot Numbers: 005985

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 250 units.

View original FDA notice →

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