Zapopan, Mexico
Oculus Technologies of Mexico, S.A. de C.V. recalls
1 recall recorded since 2018, most recently on 27 April 2026. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 27 April 2026
- Reason
- 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.
- Distribution
- US Nationwide distribution in the states of AZ, CA, CO, FL, GA, IL, IN, KY, MI, MS, NC, NJ, NY, TN, TX, UT, VA.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2275-2026
- PhaseOne Antimicrobial Solution, Model/Catalog Number: 15050
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.