Emergency Products & Research, Inc.

United Statesfrom the FDA registration address FDA establishment FEI 3002754225

Devices: 0
Registrations: FDA
FDA recalls: 11 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number: 3002754225
Address: 890 WEST MAIN STREET, KENT, OH, 44240

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 1
2025 0
2026 0

2024
- 27 Feb 2024 Z-1395-2024 Class II Ongoing Failure of adhesive to secure the pole insert. Distribution: US Nationwide distribution in the states of CA, CO, FL, GA, IL, IN, KS, MA, MI, NJ, NY, OH, OK, PA, SC, TX, UT, VA, WA.

This is an FDA establishment record without devices in deviCERTS.