medical MODERATE Updated 2026-06-10

Oculus Technologies of Mexico, S.A. de C.V. recalls PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

See all recalls from Oculus Technologies of Mexico, S.A. de C.V. →

Recalled Product

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

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Hazard / Issue

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.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: UDI:00860009268616 Lot: 25G263

✅ What Should You Do?

  1. 1Contact your healthcare provider immediately to discuss this recall.
  2. 2Stop using the device if it is safe to do so, and contact your provider.
  3. 3Follow the manufacturer's remedy instructions provided in the recall notice.
  4. 4Report device problems to FDA MedWatch or call 1-800-FDA-1088.
View official government recall