Class IIOngoingZ-0405-2026
DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month All in One Bundle
Product lacks 510(k) clearance.
- Unscented Menstrual Tampon
- No Marketing Application
DAYE (ANNE'S DAY LTD)Nov 5, 2025
The FDA has posted 29 enforcement recalls from Daye (Anne'S Day Ltd) since 2025, none of them Class I (most serious). Most recent report: Nov 5, 2025.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Product lacks 510(k) clearance.
Firm name as filed with the FDA: “DAYE (ANNE'S DAY LTD)”. Related firm entities may file under separate names. Source: U.S. FDA openFDA device enforcement reports. Informational only — verify with the FDA before acting.