Every recall we track for DAYE (ANNE'S DAY LTD) — 29 in all — plus the complaints and injury reports the public filed about them.
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.
Anne's Day recalls 9 coated and 9 nude regular tampons with model FG-TMP-RET09000900 due to lacking FDA 510(k) clearance. Consumers should check lot numbers for affected items.
Anne's Day recalls specific models of Initiation 18 Coated Super and Nude Super tampons due to lack of 510(k) clearance. Consumers should check product details and contact the company for guidance.
Anne's Day recalls 9 Coated Regular and 9 Coated Super Tampons with model FG-TMP-REF09090000 due to lacking FDA 510(k) clearance. Consumers should check lot numbers for affected products.
Anne's Day recalls All in One Bundle (model FG-BNDL-PC-REFAIO) 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 company for guidance.
Anne's Day recalls refill tampon boxes without FDA 510(k) clearance. Consumers should stop using affected models to avoid potential health risks.
Anne's Day recalls specific refill tampon models due to lack of FDA 510(k) clearance. Affected products may not meet safety standards. Consumers should check model numbers and lot codes listed in the recall notice.
Anne's Day recalls 9 coated and 9 nude regular tampons with model FG-TMP-REF09000900 due to lack of 510(k) clearance. Consumers should check lot numbers for affected items.
Anne's Day recalls Regular Flow Bundle (model FG-BNDL-PC-REFRF) due to lacking FDA 510(k) clearance. Affected units include specific lot numbers. Consumers should contact the company for details.
Anne's Day recalls 18 Coated Super Tampons (model FG-TMP-REF00180000) due to lack of FDA 510(k) clearance. Consumers should check lot numbers for affected items.
Anne's Day is recalling Initiation 18 Coated and Nude Regular tampons due to lack of FDA 510(k) clearance. Affected products have specific model numbers and lot codes. Consumers should check their items and contact the company for details.
Anne's Day is recalling Initiation 18 Coated Regular and Super Tampons with model FG-TMP-MM-IB18180000 due to lack of 510(k) clearance. Consumers should check lot numbers listed in the recall notice.
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.
Anne's Day recalls specific models of Refill 36 Coated Super Tampons due to lack of FDA 510(k) clearance. Affected products include model FG-TMP-MM-REF00360000 with listed lot numbers. Consumers should check their product details and contact the company for guidance.
Anne's Day recalls specific refill bundles due to lack of 510(k) clearance. Affected units include model FG-BNDL-PC-MM-REFHF with listed lot numbers. Consumers should check their product details and contact the company for guidance.
Anne's Day recalls specific models of refill tampons due to lack of FDA 510(k) clearance. Consumers should check model numbers and lot codes listed to determine if their product is affected.
Anne's Day Heavy Flow Bundle (model FG-BNDL-PC-REFHF) recalled due to lack of FDA 510(k) clearance. Affected units include specific lot numbers. Consumers should contact the manufacturer for details.
Anne's Day recalls Initiation 3 Month Regular Flow Bundle (model FG-BNDL-PC-MM-IBRF) due to lack of 510(k) clearance. Affected units sold with specific lot numbers. Consumers should check their product details.
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.
Anne's Day recalls Initiation 36 Coated Super Tampons with model FG-TMP-MM-IB00360000 due to lacking 510(k) clearance. Affected units include specific lot numbers. Consumers should check their product details.
Anne's Day recalls Initiation 3 Month All in One Bundle (model FG-BNDL-PC-MM-IBAIO) due to lack of 510(k) clearance. Affected units include specific lot numbers and serial codes. Consumers should check their product details.
Anne's Day recalls 3-month trial tampon boxes without FDA 510(k) clearance. Consumers should check model numbers and lot codes listed to determine if their product is affected.
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.
Anne's Day is recalling Initiation 36 Coated Regular Tampons with model FG-TMP-MM-IB36000000 due to lack of FDA 510(k) clearance. Consumers should check lot numbers for affected items.
Anne's Day recalls 18 specific lots of coated regular tampons due to lack of 510(k) clearance. Consumers should check model numbers and lot numbers for affected items.
Anne's Day recalls refill bundles with model FG-BNDL-PC-MM-REFRF due to lacking FDA 510(k) clearance. Affected units include specific lot numbers. Consumers should check their product details.
Anne's Day recalls 9 coated and 9 nude super tampons due to lack of 510(k) clearance. Consumers should check model numbers and lot numbers listed in the recall notice.
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.
Anne's Day recalls 3-month refill bundles with missing 510(k) clearance. Affected units have specific model numbers and lot codes. Consumers should check their product details to determine if they are impacted.
