Class II — DAYE (ANNE'S DAY LTD)
| Recalling firm | Daye (Anne's Day Ltd) |
|---|---|
| Registered facility | View this company's 2 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Product lacks 510(k) clearance. |
| Product | Refill 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-MM-REF18180000; |
| Quantity | 3074 packs |
| Distribution | US Nationwide distribution. |
| Initiated | 2025-02-17 |
| Classified | 2025-10-28 |
| Recall number | Z-0392-2026 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — DAYE (ANNE'S DAY LTD) (Z-0392-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97718/
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