Skip to content

Dj Orthopedics De Mexico, S.A. De C.V.

Country not established FDA establishment FEI 3006076154

Devices
0
Registrations
FDA
FDA recalls
4

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3006076154
Address
CARRETERA LIBRE TIJUANA TECATE, TIJUANA Baja California

FDA recalls4

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 4
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0
  • 2021

    • 12 Apr 2021 Z-1511-2021 Class II Terminated failed rivet at the chafe tab of arm sling. Distribution: Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United…
      Full distribution text Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United Kingdom.
    • 12 Apr 2021 Z-1512-2021 Class II Terminated failed rivet at the chafe tab of arm sling. Distribution: Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United…
      Full distribution text Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United Kingdom.
    • 12 Apr 2021 Z-1513-2021 Class II Terminated failed rivet at the chafe tab of arm sling. Distribution: Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United…
      Full distribution text Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United Kingdom.
    • 12 Apr 2021 Z-1514-2021 Class II Terminated failed rivet at the chafe tab of arm sling. Distribution: Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United…
      Full distribution text Worldwide distribution - US Nationwide distribution and the countries of Canada, France, Germany, Japan, Poland, United Kingdom.

This is an FDA establishment record without devices in deviCERTS.