Anne's Day recalls Initiation 3 Month Heavy Flow Bundle (model FG-BNDL-PC-MM-IBHF) due to lack of FDA 510(k) clearance. Affected units include specific lot numbers. Consumers should check their product details.
Product lacks 510(k) clearance.
Anne's Day is recalling its Initiation 3 Month Heavy Flow Bundle because it lacks FDA 510(k) clearance. This means the product has not been approved for safety before being sold, which could pose risks to users.
The product lacks FDA 510(k) clearance, which means it has not been tested and approved for safety by the U.S. Food and Drug Administration. Without this clearance, the product may not meet safety standards, potentially leading to health risks.
Users of the Initiation 3 Month Heavy Flow Bundle who purchased it between the dates listed in the recall notice are affected. Those with the specific model numbers and lot numbers mentioned are most at risk.
Check for the model number FG-BNDL-PC-MM-IBHF on the product. Look for the specific lot numbers listed in the recall notice, such as 20CR0014, 20CS0034, and others.
Identify the model number and lot numbers on your product to confirm if it is affected by this recall.
The product lacks FDA 510(k) clearance, meaning it has not been approved for safety before being sold.
Check the model number and lot numbers on your product to see if it is affected by this recall. If it is, you should stop using it and contact the manufacturer for further instructions.
Look for the model number FG-BNDL-PC-MM-IBHF and check the lot numbers listed in the recall notice, such as 20CR0014, 20CS0034, and others.
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-0407-2026 — Anne's Day Anne's Day Hello, I own a Anne's Day that is covered by recall Z-0407-2026 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.
