Anne's Day recalls 9 coated and 9 nude regular tampons with model FG-TMP-REF09000900 due to lack of 510(k) clearance. Consumers should check lot numbers for affected items.
Product lacks 510(k) clearance.
Anne's Day is recalling 9 coated and 9 nude regular tampons with model number FG-TMP-REF09000900 because they lack 510(k) clearance. This means the product may not meet FDA safety standards, though the recall does not indicate immediate harm to users.
The product lacks 510(k) clearance, which is a regulatory requirement for medical devices in the U.S. This means the tampons may not meet FDA safety standards, but the recall does not specify any immediate health risks or injuries.
Women who purchased the recalled tampons with model number FG-TMP-REF09000900 between 2020 and 2023 are affected. Those most at risk are users who have the specific lot numbers listed in the recall.
Check for model number FG-TMP-REF09000900 on the tampon packaging. Affected items have specific lot numbers listed in the recall, including 20CR0014 through CR003062.
Look for model number FG-TMP-REF09000900 on the tampon packaging.
Confirm if your tampons have any of the listed lot numbers, such as 20CR0014 or CR003062.
The recall states the tampons lack 510(k) clearance, but it does not indicate any immediate health risks or injuries. They may not meet FDA safety standards.
Check for model number FG-TMP-REF09000900 and any of the specific lot numbers listed in the recall, such as 20CR0014 or CR003062.
The recall does not specify a need to stop using the product immediately; it only indicates a lack of 510(k) clearance.
We’ve drafted a message you can send Anne's Day to request your refund or repair — edit it as you like.
Subject: Recall Z-0384-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0384-2026 from Anne's Day. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
