Recall
FDAHealthNovember 19, 2025

Vortex Surgical Inc. — Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;

⚠️ Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.

Is this relevant to me?

Geography
US
Source agency
FDA
Category
Health
Published
November 19, 2025

US and Japan

What's affected?

Product
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Lot code
2509040

Additional details

UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 221 units.

View original FDA notice →

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