Anne's Day recalls specific models of refill tampons due to lack of FDA 510(k) clearance. Consumers should check model numbers and lot codes listed to determine if their product is affected.
Product lacks 510(k) clearance.
Anne's Day is recalling certain refill tampon models because they lack FDA 510(k) clearance. This means the product has not been approved for safety by the U.S. Food and Drug Administration, which could pose risks to users.
The product lacks 510(k) clearance, meaning it has not been approved by the U.S. Food and Drug Administration for safety. This could lead to potential health issues if the tampons do not meet the required safety standards.
Women who purchased the specific model numbers and lot codes listed in the recall notice are affected. Those using these tampons without proper FDA clearance may face health risks.
Check for model numbers starting with FG-TMP-MM-REF00180018 or lot numbers listed in the recall notice, such as 20CR0014, 20CS0034, and others. The product is sold under the brand Anne's Day.
Look for the model number FG-TMP-MM-REF00180018 on the tampon packaging or label.
Reach out to Anne's Day customer service to confirm if your specific lot number is affected by the recall.
The product lacks FDA 510(k) clearance, meaning it has not been approved for safety by the U.S. Food and Drug Administration.
Check for the model number FG-TMP-MM-REF00180018 or lot numbers listed in the recall notice, such as 20CR0014, 20CS0034, and others.
Contact Anne's Day customer service to confirm if your specific lot number is affected by the recall.
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-0394-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0394-2026 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.
