RecallWatchUSA

Home / Recalls / Medical Devices

Oculus Technologies of Mexico, S.A. de C.V. recalls PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Recalled June 10, 2026 · FDA recall Z-2275-2026 · Oculus Technologies of Mexico, S.A. de C.V

Hazard
The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use. · FDA Class II
Units
5904 units
Sold at
US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.

Description

The recall is being conducted due to corrosion of the internal metallic spring within the sprayer component. This condition is caused by material incompatibility between the product solution and the stainless steel spring and may result in visible discoloration and the presence of trace levels of metallic elements (including iron, chromium, and nickel) in the solution during use.

Product
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Manufacturer(s)
Oculus Technologies of Mexico, S.A. de C.V.
Made in
Mexico

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