DAYE (ANNE'S DAY LTD): Device Recall
Recall #Z-0390-2026 · 02/17/2025
Class II: Risk
Recall Details
- Recall Number
- Z-0390-2026
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- DAYE (ANNE'S DAY LTD)
- Status
- Ongoing
- Date Initiated
- 02/17/2025
- Location
- London, N/A, United Kingdom
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 3074 packs
Reason for Recall
Product lacks 510(k) clearance.
Product Description
Refill 36 Coated Regular Tampons; Model Number: FG-TMP-MM-REF36000000;
Distribution Pattern
US Nationwide distribution.
Other Recalls by DAYE (ANNE'S DAY LTD)
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
- Class II: Risk 02/17/2025
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.