Drug recall
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25;
FDA recall event 98032 · Class II · Vortex Surgical Inc.
Key facts
| Event ID | 98032 |
|---|---|
| Recall numbers | Z-1004-2026 |
| Recalling firm | Vortex Surgical Inc. |
| Product type | Devices |
| Products | Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25; |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Firm Initiated |
| Reason for recall | Reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly. |
| Initiation date | Nov 19, 2025 |
| Report date | Jan 7, 2026 |
| City | Saint Charles |
| State | MO |
| Country | United States |
| FEI number | 3013002167 |
At a glance
- 1–9 Products in this recall
- 1–9 FDA inspections of this firm (FEI)
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA drug and product recalls
FDA enforcement reports list recalls of drugs, biologics, foods and other FDA-regulated products, classified by the potential health hazard.
Source: U.S. Food and Drug Administration (FDA), Enforcement Reports · Source date: