Skip to content

Emergent Protective Products USA Inc.

Country not established

Devices
3
FDA recalls
1

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What Emergent Protective Products USA Inc. makes

Emergent Protective Products USA Inc. manufactures hazardous chemical decontamination agents designed for professional use, including solutions for removing chemical contaminants from skin and equipment. Their primary product, RSDL, is formulated to neutralize and remove a range of hazardous substances, such as nerve agents and industrial toxins.

The company’s portfolio is classified under FDA’s Class I medical devices and is listed in the FDA’s Unique Device Identifier (UDI) database. The products are intended for use in emergency response and decontamination settings, adhering to regulatory standards for chemical decontamination agents in the United States.

AI-generated from registry data, 26 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue3

Newest first, rows 1-3 of 3

  • Rsdl 4002174

    None Registry: GUDID Class:I

  • Rsdl F5408ENG

    None Registry: GUDID Class:I

  • Rsdl F5402G

    None Registry: GUDID Class:I

Company details

DUNS number
079093721
Phone
1-888-773-3266

FDA recalls1

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

FDA recall records list 1 recall initiated by EMERGENT PROTECTIVE PRODUCTS USA INC., initiated on 2022-11-24. By recorded status: 1 terminated. The reasons filed fall into these groups: mechanical integrity. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.

Generated automatically from FDA recall records, as a summary of the records listed below. It describes what the records state and is not an assessment of this manufacturer.

Recalls initiated per year

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

  • 2022

    • 24 Nov 2022 Z-0773-2023 Class I Terminated Complaints of leaking packets were received. Distribution: Distribution to US state of VA (distributor), Canada, and Switzerland Submission number: K023969

Frequently asked questions

How many devices does EMERGENT PROTECTIVE PRODUCTS USA INC. have in the registry?

The registry currently lists 3 devices for EMERGENT PROTECTIVE PRODUCTS USA INC.. Devices recorded under merged duplicate company entries are counted once.

Which registries list EMERGENT PROTECTIVE PRODUCTS USA INC.'s devices?

Among its 3 most recently registered devices, EMERGENT PROTECTIVE PRODUCTS USA INC. has devices listed in FDA GUDID (3 devices).

What risk classes do EMERGENT PROTECTIVE PRODUCTS USA INC.'s devices fall under?

Among its 3 most recently registered devices, the classes recorded for EMERGENT PROTECTIVE PRODUCTS USA INC.'s devices are Class I. Each device page shows its own class and authorisation.

Are there FDA recall records for EMERGENT PROTECTIVE PRODUCTS USA INC.?

FDA recall records list 1 recall initiated by EMERGENT PROTECTIVE PRODUCTS USA INC., the most recent initiated on 2022-11-24. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from EMERGENT PROTECTIVE PRODUCTS USA INC. in the registry?

The most recently registered devices listed for EMERGENT PROTECTIVE PRODUCTS USA INC. include RSDL 4002174, RSDL F5408ENG and RSDL F5402G.

Generated automatically from registry data and not verified by a human reviewer.