Notice names this product. Oculus Technologies of Mexico’s PhaseOne Antimicrobial Solution is named in FDA Class II recall Z-2275-2026. Your particular item is not yet verified. Compare the identifiers and exclusions in the notice before deciding whether it applies. Agency-reported 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. Units affected: 5904 units. Status: Ongoing.
This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.
If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.
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…
Company / brand: Oculus Technologies of Mexico recalls
Affected product: PhaseOne Antimicrobial Solution recall status
Official ID Z-2275-2026 · Official record ↗
See all Oculus Technologies of Mexico recalls →
Found something wrong or missing? Report a data error.
Compiled from connected official public-domain government data. Sources last checked October 22, 2026 at 6:00 PM UTC.