Anne's Day recalls specific refill tampon models due to lack of FDA 510(k) clearance. Consumers should check model numbers and lot codes listed in the recall notice.
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 may not meet safety standards for medical devices, though no injuries have been reported.
The tampons lack FDA 510(k) clearance, which is required for medical devices to ensure they meet safety and performance standards. Without this clearance, the product may not function as intended or could pose risks during use, though no injuries have been reported.
Women who purchased the specific refill tampon models with model numbers starting with FG-TMP-MM-REF18001800 or the listed lot numbers. Those most at risk are users who have the product and may not be aware of the recall.
Check for model number FG-TMP-MM-REF18001800 on the tampon packaging. Look for lot numbers listed in the recall notice, such as 20CR0014, 20CS0034, and others.
Look for the model number FG-TMP-MM-REF18001800 on the tampon packaging.
Reach out to Anne's Day customer service for assistance with the recall.
The tampons lack FDA 510(k) clearance, which is required for medical devices to ensure they meet safety and performance standards.
No, the recall is for safety review, but the product may not meet FDA standards. Check the model number and lot numbers listed in the recall notice.
Check the model number on the packaging for FG-TMP-MM-REF18001800 and look for the 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-0393-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0393-2026 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.
