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

Recalled February 11, 2026 · FDA recall Z-1254-2026 · Vortex Surgical

Hazard

XXX · FDA Class II

Units

14,789 (8651 US; 6138 OUS)

Sold at

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, Netherlands, Philippines, Poland, Puerto Rico, Spain, Switzerland, Taiwan, United Kingdom, Vietnam.

Description

XXX

Product

Vortex Surgical TID Pharos Illuminated Depressor, VS0801B

Manufacturer(s)

Vortex Surgical Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →