Official recall record
PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
- Issuing authority
- US FDA — Medical Devices
- Recall initiated by firm
- 2026-04-27
- Country of alert
- Mexico
- Alert level
- Class II
- Alert type
- recall
- Barcode (EAN/GTIN)
- 00860009268616
- Brand on record
- Oculus Technologies of Mexico, S.A. de C.V.
What the authority reported
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.
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
US FDA — Medical Devices — official record →
Record last checked against the registry on 2026-09-16.
Record last checked against the registry on 2026-09-16.
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