FDA Device recall Z-1254-2026
Vortex Surgical TID Pharos Illuminated Depressor, VS0801B
- FDA Device
- Class II
- ongoing
- Published 2026-02-11
On 2026-02-11 the FDA classified a Class II recall of Vortex Surgical TID Pharos Illuminated Depressor, VS0801B by Vortex Surgical, citing XXX.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1254-2026 |
| Classification | Class II |
| Status | ongoing |
| Initiated | 2025-12-16 |
| Published | 2026-02-11 |
| Last updated | 2026-09-13 11:58 UTC |
| Company | Vortex Surgical |
| Distribution | US |
Product
Vortex Surgical TID Pharos Illuminated Depressor, VS0801B
Reason
XXX
Identifiers
| code_info | Pouch UDI 810123481309 Box UDI 810123481712 Lot 2403027R |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:58 UTC. Current status: ongoing.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1254-2026%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.