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Recall Observatory FDA recall evidence

Device product

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Z-2275-2026

April 27, 2026

Class II

Product summary

Firm
Oculus Technologies of Mexico, S.A. de C.V.
Event
Event 98959
Status
Ongoing
Classification
Class II
Quantity
5904 units
Official record key
device-enforcement:Z-2275-2026

Official wording

Reason: 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.

Code information: UDI:00860009268616 Lot: 25G263

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.

Derived failure modes

  • Unknown

    reason.no_named_rule · v1.0.0

    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.