Iantrek Inc.

Country not established FDA establishment FEI 3017891009

Devices: 0
Registrations: FDA
FDA recalls: 22 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number: 3017891009
Address: 295 Promenade Street, Suite 101, Providence, RI, 02908

FDA recalls2

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 2
2026 0

2025
- 6 Sep 2025 Z-0134-2026 Class II Ongoing Potential for compromised integrity of the sterile packaging. Distribution: US Nationwide distribution in the states of AL, AZ, CA, CT, DE, FL, GA, ID, IL, MD, MI, MN, MO, MS, NE, NJ, NY, OH, OK,…
  Full distribution text
  US Nationwide distribution in the states of AL, AZ, CA, CT, DE, FL, GA, ID, IL, MD, MI, MN, MO, MS, NE, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI.
- 6 Sep 2025 Z-0135-2026 Class II Ongoing Potential for compromised integrity of the sterile packaging. Distribution: US Nationwide distribution in the states of AL, AZ, CA, CT, DE, FL, GA, ID, IL, MD, MI, MN, MO, MS, NE, NJ, NY, OH, OK,…
  Full distribution text
  US Nationwide distribution in the states of AL, AZ, CA, CT, DE, FL, GA, ID, IL, MD, MI, MN, MO, MS, NE, NJ, NY, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WI.

This is an FDA establishment record without devices in deviCERTS.