London, N/A, United Kingdom
DAYE (ANNE'S DAY LTD) recalls
1 recall recorded since 2018, most recently on 17 February 2025. 1 is listed as ongoing. Status and classification are as published by the FDA.
Recalls1
Ongoing (FDA)1
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 17 February 2025
- Reason
- Product lacks 510(k) clearance.
- Distribution
- US Nationwide distribution.
- Initiated
- Voluntary: Firm initiated
- Recall numbers
- Z-0396-2026, Z-0393-2026, Z-0379-2026, Z-0397-2026, Z-0381-2026, Z-0399-2026, Z-0385-2026, Z-0404-2026, Z-0405-2026, Z-0400-2026, Z-0386-2026, Z-0406-2026 and 17 more
- Refill 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-REFAIO;
- Refill 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-MM-REF18001800;
- 9 Coated Super Tampons and 9 Nude Super Tampons; Model Number: FG-TMP-RET00090009;
- Refill 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-REFRF;
- 18 Coated Regular Tampons; Model Number: FG-TMP-REF18000000;
- Initiation 36 Coated Regular Tampons; Model Number: FG-TMP-MM-IB36000000;
- 9 Coated Super and 9 Nude Super Tampons; Model Number: FG-TMP-REF00090009;
- Initiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909;
- and 21 more product lines
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.