Class IIOngoingZ-0407-2026
DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month Heavy Flow Bundle
Product lacks 510(k) clearance.
DAYE (ANNE'S DAY LTD)Nov 5, 2025
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–12 of 29 recalls
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.