Anodyne Surgical

United Statesfrom the FDA registration address FDA establishment FEI 1929756

Devices: 0
Registrations: FDA
FDA recalls: 1

No devices from this company are in the catalogue yet.

Company details

FDA FEI number: 1929756
Address: 804 Corporate Centre Dr, O Fallon, MO, 63368

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 1
2022 0
2023 0
2024 0
2025 0
2026 0

2021
- 21 Apr 2021 Z-1852-2021 Class II Terminated The product may have a yellowish-brown/greenish-brown residue present at the tip of the cannula. Distribution: Worldwide distribution - US Nationwide distribution in the states of IL, NJ, TX, MO, CA, PA, WA, and the country of…
  Full distribution text
  Worldwide distribution - US Nationwide distribution in the states of IL, NJ, TX, MO, CA, PA, WA, and the country of Canada.

This is an FDA establishment record without devices in deviCERTS.