FDA Medical Device Recalls (openFDA)
DAYE (ANNE'S DAY LTD): 9 Coated Regular and 9 Coated Super Tampons; Model Number: FG-TMP-REF09090000;
- Recall number
- Z-0383-2026
- Recalling firm
- DAYE (ANNE'S DAY LTD)
- Product
- 9 Coated Regular and 9 Coated Super Tampons; Model Number: FG-TMP-REF09090000;
- Status
- Open, Classified
- Initiated
- 2025-02-17
- Posted
- 2025-10-28
- Terminated
- not on file
- Reason
- Product lacks 510(k) clearance.
- Root cause
- No Marketing Application
- Action
- On February 17, 2025 emails were sent to customers. In light of this pause, we will unfortunately need to cancel your CBD tampon subscription at this time. We understand how disappointing this news may be, and we want you to know how much we appreciate your understanding and loyalty. As a token of our gratitude, we are giving you a $20 credit which will be automatically applied to your next order. You 1II see this reflected in your total when you proceed to checkout. This credit con be used for any product on our website, including our Nude Organic Tampons, which are made with the same commitment to quality and safety you trust from Daye. We know this product has been important to many of you, and we don't want to leave you without support. Our customer core team is here to help you explore alternative options and answer any questions you may have during this transition. You can reach us by email at hello@yourdaye.com.
- Quantity
- 3074 packs
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- Model Number: FG-TMP-REF09090000; UDI-DI: 05060994741209; Lot numbers: 20CR0014, 20CS0034, 20CS0037, 20CS0038, 20CS0039, 20CS0040, 20CS0041, CR001597, CR001598, CR001599, CR001616, CR001616NR001893, CR001617, CR001617CS002165, CR001617NR001844ST23/R/3001-0523ADL, CR001617NR001902, CR001619, CR001623, CR001625, CR001625NR001844ST23/R/3001-0523ADL, CR001626, CR001627, CR001629, CR001633, CR001636, CR001638, CR001640, CR001643, CR001645, CR001655, CR001661, CR001662, CR003000, CR003001, CR003002, CR003005, CR003008, CR003009, CR003020, CR003022, CR003027, CR003031, CR003032, CR003038, CS002088, CS002119, CS002120, CS002121, CS002122, CS002143, CS002144, CS002159, CS002164, CS002164NS001653, CS002165, CS002165NS001653, CS002166, CS002166NS001648ST23/M/3001-0223ADL, CS002167, CS002168, CS002169, CS002177, CS002181, CS002183, CS002195, CS002196, CS003005, CS003015, CS003016, CS003022, CS003034, CS003048, CS003049, CS003050, CS003052, CS003053, CS003054, CS003055, CS003057, CS003062, CS003081, CR001615, CR001616CS002163NR001890NS001649, CR001616CS002163NR001892NS001650, CR001616CS002164, CR001617CS002165, CR001655CS002196, CS002163, CS002164, CR001661NR002015, CS003005NS001775, CR003000, CS003005, CS003016, CS003022, CR003000, CR003000, CR003000NR002173, CS003022NS001781.
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- HEB
- Firm FEI
- 3036679730
- Firm city
- London
- Firm state
- not on file
- Firm country
- United Kingdom
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28