Home/Recalls/FDA-Z-2275-2026
FDA DevicesClass II

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Published: June 10, 2026Recall ID: Z-2275-2026Category: devicesCountry: US

Reason for Recall / Hazard

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.

Product Description & Identification

PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050

Additional Source Details

FieldValue
CityZapopan
Event id98959
Address 1Calle Industria Vidriera 81
Address 2Industrial Zapopan Norte
Code infoUDI:00860009268616 Lot: 25G263
Postal codeN/A
Report date20260610
Product typeDevices
Product quantity5904 units
Reason for recallThe 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.
Voluntary mandatedVoluntary: Firm initiated
Recall initiation date20260427
Center classification date20260601

Overview

  • Recalling FirmOculus Technologies of Mexico, S.A. de C.V.
  • StatusOngoing
  • Risk LevelClass II
  • DistributionUS Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.
Official Agency Alert