FDA recall, , Moderate risk
PhaseOne Antimicrobial Solution
PhaseOne Antimicrobial Solution has corrosion of its internal spring, which may cause discoloration and trace metals in the solution.
Summary by Recall Canary from the FDA notice
What happened
Oculus Technologies of Mexico, S.A. de V.C., of Zapopan, Mexico, is recalling PhaseOne Antimicrobial Solution because corrosion of the internal metallic spring within the sprayer component may result in visible discoloration and the presence of trace levels of metallic elements, including iron, chromium, and nickel, in the solution during use. The condition is caused by material incompatibility between the product solution and the stainless steel spring.
The recall affects 5904 units distributed in Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Kentucky, Michigan, Mississippi, North Carolina, New Jersey, New York, Tennessee, Texas, Utah, and Virginia. The company began the recall on April 27, 2026, and the FDA added it to its Enforcement Report on June 1, 2026.
What to do
We don't have product-specific instructions for this recall. FDA's general advice for medical device recalls:
- A device recall doesn't always mean you must stop using it: it may need to be checked, adjusted or fixed.
- Talk to your health care provider before you stop using it.
Is yours affected?
Match the model number, UDI-DI and lot code listed under your product.
A UDI-DI is the device identifier printed with the barcode on the device label.
PhaseOne Antimicrobial Solution
- Model number
- 15050
- UDI-DI
- 00860009268616
- Lot code
- 25G263
Recall details
- Company began the recall
- Sold in
US Nationwide distribution in the states of Arizona, California, Colorado, Florida, Georgia, Illinois, Indiana, Kentucky, Michigan, Mississippi, North Carolina, New Jersey, New York, Tennessee, Texas, Utah, Virginia.
- Company
- Oculus Technologies of Mexico, S.A. de C.V.Zapopan, Mexico
- Hazard
- Foreign object
- Risk
Moderate risk
Using it may cause short-term health problems, or ones that treatment can reverse. Serious harm is unlikely.
FDA Class II recall · How risk is rated
- Event ID
- 98959
- Recall number
- Z-2275-2026
- Quantity recalled
- 5904 units
Timeline
FDA's Enforcement Report is its public list of recalls; FDA adds a recall when it posts it and publishes the list weekly.
Company began the recall
Added to FDA's Enforcement Report · Classified by FDA
Listed on Recall Canary
In FDA's weekly enforcement report
Summary updated
