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FDAApril 27, 2026device

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Official recall recorded by the U.S. Food & Drug Administration.

The 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.

What to do

FDA enforcement status: Ongoing

Brands named

oculus technologiesoculus

UPCs

00860009268616

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050 — Recall Details · AllClear