Anne's Day recalls 9 coated and 9 nude super tampons due to lack of 510(k) clearance. Consumers should check model numbers and lot numbers listed in the recall notice.
Product lacks 510(k) clearance.
Anne's Day is recalling 9 coated and 9 nude Super Tampons because they lack 510(k) clearance. This means the product may not meet safety standards for medical devices, though no injuries have been reported.
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 safety standards, potentially leading to health risks if used improperly.
Owners of the recalled Super Tampons with model number FG-TMP-RET00090009 and specific lot numbers listed in the recall notice are affected. People using these products for medical purposes may be at risk.
Check for model number FG-TMP-RET00090009 and lot numbers like 20CR0014, 20CS0034, or CR001597 on the product packaging. The recall includes specific batches listed in the official notice.
Look for the model number FG-TMP-RET00090009 and lot numbers listed in the recall notice to confirm if your tampons are affected.
The product lacks 510(k) clearance, a regulatory requirement for medical devices in the U.S. This means it may not meet safety standards.
Check the model number and lot numbers listed in the recall notice to see if your tampons are affected. If they are, you should stop using them.
The recall notice does not mention any injuries or health issues associated with this product.
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-0379-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0379-2026 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.
