Vortex Surgical Inc. recalls Vortex Surgical TID Pharos Illuminated Depressor, VS0801B

Recall date

December 16, 2025

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-1254-2026

FDA classification

Class II

Brand / firm

Vortex Surgical Inc.

Sold / distributed

Worldwide Distribution: US (nationwide) to states of: AL, AR, AZ, CA, CT, FL, HI, IA, IL, IN, KY, MA, MI, MN, MS, NC, NE, NJ, NM, NY, OH, OR, PA, RI, SC, SD, TN, TX, WA, WI, VA; and OUS (foreign) to countries of: Australia, Chile, China, France, Germany, India, Ireland, Italy, Japan, Korea, Mexico,…

Why it was recalled

XXX

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Vortex Surgical TID Pharos Illuminated Depressor, VS0801B