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 to determine if their product is affected.
Product lacks 510(k) clearance.
Anne's Day is recalling certain refill tampon models because they do not have the required FDA 510(k) clearance. This means the product may not be safe for use as intended, though the recall does not specify immediate health risks.
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 and could pose potential risks during use, though the exact hazard is not specified in the recall.
Women who purchased the specific refill tampon models with model numbers starting with FG-TMP-MM-REF18180000 or the listed lot numbers are affected. Those using these products for menstrual care are most at risk.
Check for model numbers starting with FG-TMP-MM-REF18180000 or lot numbers listed in the recall (e.g., 20CR0014, 20CS0034, etc.). The product is sold under the brand Anne's Day.
Look for the model number on the tampon packaging or label to see if it matches the listed model numbers (e.g., FG-TMP-MM-REF18180000).
Reach out to Anne's Day customer service to confirm if your specific product is affected and get guidance on next steps.
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.
Check the model number on the packaging or label. Affected products have model numbers starting with FG-TMP-MM-REF18180000 or the listed lot numbers (e.g., 20CR0014, 20CS0034).
Contact Anne's Day customer service to confirm if your product is affected and get guidance on next steps. The recall does not specify a return or disposal process.
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-0392-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0392-2026 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.
