DAYE (ANNE'S DAY LTD) recalls

29 recalls on record · latest: February 17, 2025

Official U.S. recall history for DAYE (ANNE'S DAY LTD), compiled from official government records.

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DAYE (ANNE'S DAY LTD) recalls Refill 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-MM-REF18180000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls 9 Coated Regular Tampons and 9 Nude Regular Tampons; Model Number: FG-TMP-RET09000900;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-MM-IB00180018;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls 9 Coated Regular and 9 Coated Super Tampons; Model Number: FG-TMP-REF09090000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls All in One Bundle; Model Number: FG-BNDL-PC-REFAIO;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-REF09090909;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 36 Coated Regular Tampons; Model Number: FG-TMP-MM-REF36000000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls 9 Coated Regular and 9 Nude Regular Tampons; Model Number: FG-TMP-REF09000900;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Regular Flow Bundle; Model Number: FG-BNDL-PC-REFRF;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls 18 Coated Super Tampons; Model Number: FG-TMP-REF00180000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-MM-IB18001800;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 18 Coated Regular and 18 Coated Super Tampons; Model Number: FG-TMP-MM-IB18180000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-IBHF;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 36 Coated Super Tampons; Model Number: FG-TMP-MM-REF00360000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 3 Month Heavy Flow Bundle; Model Number: FG-BNDL-PC-MM-REFHF;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 18 Coated Super and 18 Nude Super Tampons; Model Number: FG-TMP-MM-REF00180018;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Heavy Flow Bundle; Model Number: FG-BNDL-PC-REFHF;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-IBRF;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Trial Tampon Box; Model Number: FG-TMP-REF04050504;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 36 Coated Super Tampons; Model Number: FG-TMP-MM-IB00360000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-IBAIO;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 3 Month Trial Tampon Box; Model Number: FG-TMP-MM-IB09090909;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls 9 Coated Super and 9 Nude Super Tampons; Model Number: FG-TMP-REF00090009;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Initiation 36 Coated Regular Tampons; Model Number: FG-TMP-MM-IB36000000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls 18 Coated Regular Tampons; Model Number: FG-TMP-REF18000000;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 3 Month Regular Flow Bundle; Model Number: FG-BNDL-PC-MM-REFRF;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls 9 Coated Super Tampons and 9 Nude Super Tampons; Model Number: FG-TMP-RET00090009;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 18 Coated Regular and 18 Nude Regular Tampons; Model Number: FG-TMP-MM-REF18001800;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.

DAYE (ANNE'S DAY LTD) recalls Refill 3 Month All in One Bundle; Model Number: FG-BNDL-PC-MM-REFAIO;

February 17, 2025 · Medical device recalls Moderate risk Product lacks 510(k) clearance.