Daye (Anne's Day Ltd)
1 recall(s) on record — most severe on record: Class II.
Recalls by year
- Recalls (1)
Registered facilities (2)
- Tampon Innovations FEI 3028725772 · BG
- DAYE (ANNE'S DAY LTD) FEI 3036679730 · GB
Recalls & enforcement
- Class IIOngoing2025-02-17Product lacks 510(k) clearance.
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.
Cite this record
RegWarden. “Daye (Anne's Day Ltd) — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-10088636-daye-anne-s-day-ltd/
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