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DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom Recalls

All product recalls associated with DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom.

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 221–240 of 4465 recalls

Daye Tampon Initiation Mix (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Regular Flow Bundle (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Heavy Flow Bundle (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide

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• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Trial Tampon Box (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Tampon Combination (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Regular Flow Refill (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Refill Bundle (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Trial Box Refill (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Super Tampons (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Regular Tampons (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye All-in-One Bundle (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Regular Tampons Initiation (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Daye Trial Box Initiation (Daye) – 510(k) Clearance Missing (2025)

Product lacks 510(k) clearance.

FDAFeb 17, 2025Nationwide• DAYE (ANNE'S DAY LTD) Biscuit Factory Business Complex 100 Drummond Road London United Kingdom

Aveir DR Leadless Pacemaker (Abbott) – Battery Temperature Risk (2025)

Due to a manufacturing issue, leadless pacemakers may have been exposed to higher than normal temperatures which may result in premature battery failure.

FDAFeb 15, 2025Nationwide• Abbott Medical

Terberg YT Series (Terberg) – steering arm bolt (2025)

Terberg Benschop B.V. (Terberg Benschop) is recalling certain 2023-2024 YTXX3 vehicles. A steering arm bolt may have been improperly tightened.

NHTSAFeb 12, 2025Nationwide• TERBERG BENSCHOP B.V.

Origin Data Management Software (Brainlab) – patient record merge (2025)

Under certain circumstances, it can occur that patient records from unrelated individuals are automatically merged into one patient record without user notification.

FDAFeb 10, 2025Nationwide• Brainlab AG Olof-Palme-Str. 9 Munich Germany

Latanoprost (Aspen Biopharma) – CGMP Deviation (2025)

CGMP Deviations

Class IIModerate

FDAFeb 7, 2025FL, IN• Aspen Biopharma Labs Pvt., Ltd.

Chlorambucil (Aspen Biopharma) – CGMP Deviation (2025)

CGMP Deviations

Class IIModerate

FDAFeb 7, 2025FL, IN• Aspen Biopharma Labs Pvt., Ltd.

Finasteride (Aspen Biopharma) – CGMP Issues (2025)

CGMP Deviations

Class IIModerate

FDAFeb 7, 2025FL, IN• Aspen Biopharma Labs Pvt., Ltd.

Voriconazole (Aspen Biopharma) – CGMP Issues (2025)

CGMP Deviations

Class IIModerate

FDAFeb 7, 2025FL, IN• Aspen Biopharma Labs Pvt., Ltd.