Anne's Day recalls refill tampon boxes without FDA 510(k) clearance. Consumers should stop using affected models to avoid potential health risks.
Product lacks 510(k) clearance.
Anne's Day is recalling refill tampon boxes that lack FDA 510(k) clearance. This means the product may not be safe for use and could pose health risks to users.
The product lacks FDA 510(k) clearance, which is required for medical devices to ensure safety and effectiveness. Without this clearance, the tampon box may not meet the necessary standards for use, potentially leading to health issues.
Women who purchased the recalled refill tampon boxes are affected. Those using the product without proper regulatory clearance may face health risks.
Check for model number FG-TMP-MM-REF09090909 on the tampon box. Affected units have specific lot numbers listed in the recall notice.
Immediately stop using the recalled tampon boxes as they lack FDA 510(k) clearance.
The product lacks FDA 510(k) clearance, which is required for medical devices to ensure safety and effectiveness.
Affected model numbers include FG-TMP-MM-REF09090909 and specific lot numbers listed in the recall notice.
Check the model number on the tampon box; affected units have model number FG-TMP-MM-REF09090909 and specific lot numbers listed in the recall notice.
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-0395-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0395-2026 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.
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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.
