Medical Device Recall: PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Oculus Technologies of Mexico, S.A. de C.V. · April 27, 2026
Reason for Recall
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.
Distribution
US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.
States Affected
NATIONWIDE
Quantity Affected
5904 units
Source: FDA (openFDA Device Enforcement)
Recall number: Z-2275-2026
Status: ongoing
SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.