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Laerdal Medical (Suzhou) Co., Ltd.

Country not established FDA establishment FEI 3004993040

Devices
0
Registrations
FDA
FDA recalls
1

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3004993040
Address
NO.19 BLDG., HUOJU RD., 215009 SUZHOU JIANGSU PROVINCE

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 1
  • 2021 0
  • 2022 0
  • 2023 0
  • 2024 0
  • 2025 0
  • 2026 0

  • 2020

    • 18 Dec 2020 Z-0868-2021 Class II Terminated Component failures may cause the unit to lose all suction. Users will need to obtain alternate suction devices or methods, leading to a delay in treatment and, in worst case scenario, potential suffocation if alternative suction or ventilation method is not administered by the user. Distribution: Worldwide distribution - US Nationwide distribution. Submission number: K120065

This is an FDA establishment record without devices in deviCERTS.