Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
| Source | FDA Device Enforcement |
|---|---|
| Category | Medical Device |
| Severity | Medium |
| Status | ongoing |
| Recall date | November 19, 2025 |
| Reported | January 07, 2026 |
| Recalling firm | Vortex Surgical Inc. |
| Country / region | United States MO |
Hazard
Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Affected products
- Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
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