Anne's Day recalls 9 specific models of coated and nude super tampons due to lack of FDA 510(k) clearance. Consumers should check model numbers and lot numbers listed to determine if their product is affected.
Product lacks 510(k) clearance.
Anne's Day is recalling 9 specific models of coated and nude super tampons because they lack FDA 510(k) clearance. This means the products were not properly tested for safety before being sold, which could pose risks to users.
The tampons lack FDA 510(k) clearance, meaning they were not tested for safety by the U.S. Food and Drug Administration before being sold. This could lead to potential health risks if the products are used without proper safety validation.
Women who purchased the recalled tampons between 2020 and 2023 are likely affected. Those using the specific model numbers and lot numbers listed in the recall are at the highest risk.
Check for model numbers starting with FG-TMP-REF00090009 or lot numbers listed in the recall, such as 20CR0014, 20CS0034, and others. The recall covers specific batches sold between 2020 and 2023.
Look for model numbers starting with FG-TMP-REF00090009 on the tampon packaging.
Reach out to Anne's Day directly to confirm if your specific model or lot number is affected.
The tampons lack FDA 510(k) clearance, meaning they were not properly tested for safety before being sold.
Check the model number on the packaging for FG-TMP-REF00090009 or look for the specific lot numbers listed in the recall notice.
Contact Anne's Day directly to confirm if your specific model or lot number is affected. They will provide guidance on next steps.
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-0385-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0385-2026 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.
