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Sarnova Hc, LLC

Country not established FDA establishment FEI 3014680755

Devices
0
Registrations
FDA
FDA recalls
55 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3014680755
Address
5000 Bradenton Ave, Dublin, OH, 43017

FDA recalls5

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 2
  • 2024 2
  • 2025 0
  • 2026 1

  • 2026

    • 12 Jun 2026 Z-0144-2027 Not yet classified Ongoing Affected kits were assembled with pediatric nasal cannula instead of the intended adult nasal cannula. Distribution: US Nationwide distribution in the states of IA, IL, IN, KY, MI, MN, MO, ND, OH, UT.

  • 2024

    • 12 Feb 2024 Z-1307-2024 Class II Ongoing Endotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube. Distribution: US Nationwide distribution.
    • 12 Feb 2024 Z-1308-2024 Class II Ongoing Endotracheal Tube Holder included in certain kits is not compatible with a nasal intubation procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube. Distribution: US Nationwide distribution.

  • 2023

    • 6 Nov 2023 Z-0720-2024 Class II Ongoing It was determined that the Endotracheal Tube Holder included in certain kits is not compatible with a cricothyrotomy procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube. Distribution: US Nationwide
    • 6 Nov 2023 Z-0721-2024 Class II Ongoing It was determined that the Endotracheal Tube Holder included in certain kits is not compatible with a cricothyrotomy procedure, leaving practitioners without the necessary means to secure the inserted endotracheal tube. Distribution: US Nationwide

This is an FDA establishment record without devices in deviCERTS.