Oculus Technologies of Mexico recalls

Recall found. Oculus Technologies of Mexico is named in FDA Class II recall Z-2275-2026 covering PhaseOne Antimicrobial Solution. 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. Identifying details: UDI:00860009268616 Lot: 25G263. Status: Ongoing.

Models with recalls

PhaseOne Antimicrobial Solution (1)

All Oculus Technologies of Mexico recalls

FDA Class II · Medical device · June 10, 2026

PhaseOne Antimicrobial Solution recall — Oculus Technologies of Mexico, S.A. de C.V.

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 produc…

Official ID Z-2275-2026 · Official record ↗

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Compiled from official public-domain government data. Last checked October 22, 2026 at 6:00 PM UTC.