Oculus recalls PhaseOne Antimicrobial Solution Model 15050 due to internal spring corrosion from material incompatibility, causing metallic discoloration and trace metal contamination.
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.
Oculus is recalling its PhaseOne Antimicrobial Solution (Model 15050) because corrosion in the internal spring can cause visible discoloration and trace metal contamination in the solution. This poses a risk of metal particles entering the solution during use.
The product contains a stainless steel spring that corrodes when exposed to the antimicrobial solution. This corrosion causes visible discoloration and releases trace amounts of metals like iron, chromium, and nickel into the solution during use.
Users of the PhaseOne Antimicrobial Solution Model 15050 are affected. Those using the product for medical or industrial purposes may be at higher risk due to potential metal contamination.
Check for the model number 15050 on the product label. The product was sold with UDI:00860009268616 and lot number 25G263.
Verify the model number 15050 and lot number 25G263 on the product label.
The recall is due to corrosion of the internal metallic spring caused by material incompatibility between the product solution and stainless steel spring, which may result in visible discoloration and trace metal contamination.
The recall record does not specify a remedy, so no action is required beyond checking product details.
The recall record states the hazard involves discoloration and trace metal contamination but does not mention injury risks, so the danger level is low risk.
We’ve drafted a message you can send Oculus Technologies to request your refund or repair — edit it as you like.
Subject: Recall Z-2275-2026 — Oculus Technologies Oculus Technologies Hello, I own a Oculus Technologies that is covered by recall Z-2275-2026 from Oculus Technologies. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
