← FDA ENFORCEMENT
Z-2275-2026Class II

Oculus Technologies of Mexico, S.A. de C.V.

Recalling firm
Oculus Technologies of Mexico, S.A. de C.V.
Product type
Device
Status
Ongoing
Report date
2026-06-10
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.
Product quantity
5904 units
Initiated by
Voluntary: Firm initiated
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.

Product description

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Code / lot info

UDI:00860009268616 Lot: 25G263

Data: U.S. FDA openFDA enforcement API. Recall details are as reported by the FDA. The quality-domain mapping and severity are a SPEQ editorial interpretation of the recall reason, not an official FDA classification.