FDA Device recall Z-1004-2026
Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25
- FDA Device
- Class II
- ongoing
- Published 2026-01-07
On 2026-01-07 the FDA classified a Class II recall of Vortex Surgical 25ga Illuminated Flex-Tip Laser Probe, Catalog Number VS0135.25 by Vortex Surgical, citing reason for the voluntary recall is some products in this lot are not passing through a 25ga cannula smoothly.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1004-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-11-19 |
| Published | 2026-01-07 |
| Last updated | 2026-09-13 11:57 UTC |
| Company | Vortex Surgical |
| Distribution | n/a |
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.
Identifiers
| code_info | UDI: Box (01)00810123483617(17)281001(10)2509040, Pouch (01)00810123483549(17)281001(10)2509040. Lot Number 2509040 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:57 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1004-2026%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.