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Medical Device

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Recall date: 2026-06-10 · Source: FDA_DEVICE
Brand / Firm
Oculus Technologies of Mexico, S.A. de C.V.
Product
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
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.
Units affected
5904 units
Description
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
View official recall notice →