Skip to content

Oculus Technologies of Mexico, S.A de C.V.

Country not established FDA establishment FEI 3007244484

Devices
0
Registrations
FDA
FDA recalls
11 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3007244484
Address
Industria Vidriera 81, Zapopan Jalisco

FDA recalls1

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Recalls initiated per year

  • 2017 0
  • 2018 0
  • 2019 0
  • 2020 0
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 1

  • 2026

    • 27 Apr 2026 Z-2275-2026 Class II Ongoing 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. Submission number: K172851

This is an FDA establishment record without devices in deviCERTS.