Anne's Day recalls Trial Tampon Box model FG-TMP-REF04050504 due to lack of FDA 510(k) clearance. Affected units include specific lot numbers and model variants. Consumers should check their product details and contact the manufacturer for guidance.
Product lacks 510(k) clearance.
Anne's Day is recalling its Trial Tampon Box with model number FG-TMP-REF04050504 because it lacks 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 during use.
The product lacks FDA 510(k) clearance, meaning it has not been approved for safety by the U.S. Food and Drug Administration. This could result in potential safety issues during use, though specific risks are not detailed in the recall notice.
Women who purchased the Trial Tampon Box with model number FG-TMP-REF04050504 are likely affected. Those using the product for menstrual care may be at risk if the device has not been cleared by the FDA.
Check for the model number FG-TMP-REF04050504 on the product. Affected units include specific lot numbers listed in the recall notice, such as 20CR0014, 20CS0034, and others.
Look for the model number FG-TMP-REF04050504 and the listed lot numbers on the product.
The product lacks FDA 510(k) clearance, meaning it has not been approved for safety by the U.S. Food and Drug Administration.
Check the product details for the model number and lot numbers. If you have the affected model, contact Anne's Day for guidance.
The recall notice states the product lacks FDA 510(k) clearance, but specific injury risks are not detailed in the official 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-0386-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0386-2026 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.
