Vortex Surgical Inc. recalls Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe
- Recalling company
- Vortex Surgical Inc.
- Product
- Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
- Reason
- Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
- Classification
- Class II – may cause temporary or medically reversible health consequences
- Recall date
- Nov 19, 2025
- Reported
- Jan 7, 2026
- Distribution
- US and Japan
- Status
- Ongoing
- Quantity
- 221 units
- Lot / codes
- UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040
- Company location
- Saint Charles, MO
- Recall type
- Voluntary: Firm initiated
- Recall number
- Z-1004-2026
- Agency
- U.S. Food and Drug Administration (FDA)
View official FDA notice ↗ Search recall number Z-1004-2026 in the FDA Enforcement Report. Also see FDA recall press releases.
If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.