Recall Z-0404-2026— DAYE (ANNE'S DAY LTD)
Class II · Ongoing
Class II FDA medical device recall by DAYE (ANNE'S DAY LTD), initiated 2025-02-17. FDA's recall record names no specific 510(k) clearance for this event. Product: Initiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909;. Reason: Product lacks 510(k) clearance..
- Recalling firm
- DAYE (ANNE'S DAY LTD)
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2025-02-17
- Firm location
- London, N/A, United Kingdom
Product description
Initiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909;
Reason for recall
Product lacks 510(k) clearance.
Data sourced from openFDA. This site is unofficial and independent of the FDA.