Recall archive / FDA device enforcement
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25; — FDA record Z-1004-2026
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Nov 19, 2025. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- 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
- Recalling firm
- Vortex Surgical Inc.
- Quantity
- 221 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1004-2026
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040 |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
US and Japan
No US distribution state could be established from this record. Check the official notice.
Dates in the source
- Report date
- Jan 7, 2026
- Recall initiation date
- Nov 19, 2025
- Center classification date
- Dec 30, 2025
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.