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PhaseOne Antimicrobial Solution Sprayer
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MEDICAL DEVICE RECALLMODERATE

PhaseOne Antimicrobial Solution Sprayer

Oculus Technologies is recalling PhaseOne Antimicrobial Solution due to sprayer spring corrosion that may contaminate the product.

What to do

Stop using the affected product immediately and contact the manufacturer for further instructions regarding replacement or disposal.

Recalled
Listed
Updated
Recall No.
Z-2275-2026
Agency
FDA
Firm
Oculus Technologies of Mexico, S.A. de C.V.
Recall ID
98959
Status
ONGOING

Recall at a glance

Quantity recalled
5904 units

Why it was recalled

Oculus Technologies is recalling the PhaseOne Antimicrobial Solution due to corrosion of the internal metallic spring within the sprayer component. This material incompatibility may cause discoloration and introduce trace levels of iron, chromium, and nickel into the solution during use.

Is mine affected?

Check the model, lot, or serial number on the device or its packaging. Yours is affected if it matches one below.

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Lot code
25G263
UDI-DI
00860009268616

Where it was sold

Distributed nationwide.

Timeline

  1. Firm initiated recall
  2. Publicly announced
  3. Listed on Recall Canary
  4. Summary updated

Official source

View on U.S. Food and Drug Administration →

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Editorial summary by Recall Canary · summary updated 2026-06-02 · primary source: U.S. Food and Drug Administration · severity reflects the agency's published classification