Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Reported: January 7, 2026 Initiated: November 19, 2025 #Z-1004-2026
Product Description
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
Reason for Recall
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Details
- Recalling Firm
- Vortex Surgical Inc.
- Units Affected
- 221 units
- Distribution
- US and Japan
- Location
- Saint Charles, MO
Frequently Asked Questions
What product was recalled? ▼
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;. Recalled by Vortex Surgical Inc.. Units affected: 221 units.
Why was this product recalled? ▼
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on January 7, 2026. Severity: Moderate. Recall number: Z-1004-2026.
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