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Daye (Anne's Day Ltd)

Country not established FDA establishment FEI 3036679730

Devices
0
Registrations
FDA
FDA recalls
2929 ongoing

No devices from this company are in the catalogue yet.

Company details

FDA FEI number
3036679730
Address
4th Floor, London London, City of

FDA recalls29

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 29
  • 2026 0

Showing the 10 most recent of 29 recalls.

  • 2025

    • 17 Feb 2025 Z-0379-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0380-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0381-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0382-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0383-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0384-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0385-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0386-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0387-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0388-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
Show the 25 most recent of 29 recalls

  • 2025

    • 17 Feb 2025 Z-0389-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0390-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0391-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0392-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0393-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0394-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0395-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0396-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0397-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0398-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0399-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0400-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0401-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0402-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.
    • 17 Feb 2025 Z-0403-2026 Class II Ongoing Product lacks 510(k) clearance. Distribution: US Nationwide distribution.

This is an FDA establishment record without devices in deviCERTS.