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CLASS II · ModerateFDA

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

📅 Apr 27, 2026 · 📍 Nationwide
Recalling company
Oculus Technologies of Mexico, S.A. de C.V.
Product
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
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.
Classification
Class II – may cause temporary or medically reversible health consequences
Recall date
Apr 27, 2026
Reported
Jun 10, 2026
Distribution
US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.
Status
Ongoing
Quantity
5904 units
Lot / codes
UDI:00860009268616 Lot: 25G263
Company location
Zapopan
Recall type
Voluntary: Firm initiated
Recall number
Z-2275-2026
Agency
U.S. Food and Drug Administration (FDA)

View official FDA notice ↗ Search recall number Z-2275-2026 in the FDA Enforcement Report. Also see FDA recall press releases.

If you use this product, check the lot, NDC or model number against the official notice and follow its instructions. Do not stop a prescribed medicine or remove a medical device without talking to your doctor or pharmacist. Report problems to FDA MedWatch. FoodRecallNow summarizes public FDA data and is not medical advice.