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PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Class II
Recalling firm
Oculus Technologies of Mexico, S.A. de C.V.
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.
Affected products (lot / model / serial)
UDI:00860009268616 Lot: 25G263
Units affected
5904 units
Distribution pattern
US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.
Firm location
Zapopan, Mexico
Recall type
Voluntary: Firm initiated
Product type
Devices
Status
Ongoing
Recall number
Z-2275-2026
Recall initiated
April 27, 2026
FDA classification date
June 1, 2026
FDA report date
June 10, 2026
FDA event ID
98959
Last updated on HTM Vibe
July 23, 2026
View on openFDA