Vortex Surgical TID Pharos Illuminated Depressor — Class II medical device recall Z-1254-2026
Ongoing recall by Vortex Surgical Inc., reported 2026-02-11, distributed nationwide. XXX
| Recall number | Z-1254-2026 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Vortex Surgical Inc., Saint Charles, MO, United States |
| Recall initiated | 2025-12-16 |
| Classified | 2026-02-04 |
| Reported by FDA | 2026-02-11 |
| Distributed | Nationwide (US) |
| Countries outside the US | AU, CH, CL, CN, DE, ES, FR, GB, IE, IN, IT, JP, KR, MX, NL, PH, PL, TW, VN |
| UPC / GTIN / UDI-DI | 00810123481309, 00810123481712 |
| Lot numbers | 2403027R |
Product
Vortex Surgical TID Pharos Illuminated Depressor, VS0801B
Reason for recall
XXX
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1254-2026. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.