🔍 RecallPedia

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Class I - Dangerous
🏥 Medical Devices Recalled: April 27, 2026 Oculus Technologies of Mexico, S.A. de C.V. Other Medical Devices Nationwide

What Should You Do?

  1. Check if you have this product:
    UDI:00860009268616 Lot: 25G263
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Oculus Technologies of Mexico, S.A. de C.V.
Reason for Recall:
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.
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
ongoing

Product Information

Full Description:

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Product Codes/Lot Numbers:

UDI:00860009268616 Lot: 25G263

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-2275-2026