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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

442

Class I (Serious)

138

Most Recent

Dec 2025

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 401–420 of 7663 recalls

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

Product lacks 510(k) clearance.

Low

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.

Low

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

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

Product lacks 510(k) clearance.

Low

FDAFeb 17, 2025Nationwide

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• 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.

Low

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.

Low

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.

Low

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.

Low

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.

Low

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.

Low

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

Cybex Eos Travel System (Cybex) – Harness Safety Concern (2025)

Columbus Trading-Partners USA, Inc. (CTP) is recalling certain Cybex Aton G, Aton G SensorSafe, Aton G Swivel, Aton G Swivel SensorSafe, Eos and Aton G Swivel Travel System, Eos and Aton G Travel System, Libelle and Aton G Travel System, and Beezy and Aton G Travel System child seats. The harness hip anchorage retention hooks may bend, causing the anchor pin to loosen, and the harness strap to detach.

High

NHTSAFeb 14, 2025Nationwide• CYBEX

Mercedes-Benz eSprinter (Mercedes-Benz) – Axle Weld Concern (2025)

Daimler Vans USA, LLC (DVUSA) is recalling certain 2024 Mercedes-Benz eSprinter vehicles. The welds on the helical gear within the rear axle drivetrain may fail, causing a loss of drive power.

High

NHTSAFeb 14, 2025Nationwide• MERCEDES-BENZ

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.

High

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

Mercedes-Benz EQB 350 (Mercedes-Benz) – battery issue (2025)

Fire/Burn Risk

Mercedes-Benz USA, LLC (MBUSA) is recalling certain 2022-2025 EQB 250, EQB 300 4MATIC, and EQB 350 4MATIC electric vehicles. The high voltage battery may fail internally and lead to a vehicle fire while parked or driving.

High

NHTSAFeb 7, 2025Nationwide• MERCEDES-BENZ

Ariens Snow Throwers (Ariens) – Laceration Risk (2025)

Laceration Risk

This recall involves certain Ariens DELUXE-, PLATINUM- and PROFESSIONAL-series Sno-Thro® models. The recalled snow throwers were sold in a bright orange color and are equipped with either rear wheels or tracks. The model and serial numbers are located on the white square ID tag on the frame. Some recalled snowblowers have already been inspected and repaired. Consumers are urged to visit https://www.ariensco.com/safetyrecall for a list of recalled units.

High

CPSCFeb 6, 2025Nationwide• Ariens Company, of Brillion, Wisconsin

Rotarex Atherectomy System (Bard) – catheter breakage (2025)

Atherectomy Catheter eIFU updated to clarify and emphasize procedural steps intended to reduce the likelihood of catheter breakage events. Catheter has an outer cylinder connected to a rotating helix, which could fracture and/or break, which would require retrieval, and helix facture/break could cause vessel injury and lead to severe bleeding.

High

FDAFeb 5, 2025Nationwide• Bard Peripheral Vascular Inc 1625 W 3rd St Bldg 1 850 W. Rio Salado Prkwy. Tempe AZ 85281-2438

IntelePACS Software (Intelerad) – image calculation error (2025)

A software application that receives digital images and data from various sources has a bug in specific software versions that will calculate the Standard Uptake Value (SUV) incorrectly for PET/CT studies acquired on the days of Daylight Savings Time (DST); only on dates in which DST transition occurs; all other dates are unaffected. An incorrect SUV may lead to an incorrect diagnosis.

High

FDAFeb 5, 2025Nationwide• INTELERAD MEDICAL SYSTEMS INCORPORATED 800, Boul. de Maisonneuve Est 12th floor Montreal Canada

Optima MR360 MRI System (GE Healthcare) – SAR monitoring (2025)

For certain MR systems, a scan can be resumed following a Power Monitor trip when the "6-minute average SAR" is above the limit indicated on the "SAR Display". The user interface may incorrectly enable a scan to proceed earlier than intended. If resumed by the operator, such a scan can result in potential excessive tissue heating, especially if the patient is in contact with a conductive material or has an implant.

Moderate

FDAJan 31, 2025Nationwide• GE Healthcare (China) Co., Ltd. 1F-5F BLD 1, No.1 Tongji South Road, Beijing Economic-Technological Development Area Beijing China

Stay Informed

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

Recall Summary

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

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

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

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

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

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

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

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

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

Cybex Eos Travel System (Cybex) – Harness Safety Concern (2025)

Mercedes-Benz eSprinter (Mercedes-Benz) – Axle Weld Concern (2025)

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

Mercedes-Benz EQB 350 (Mercedes-Benz) – battery issue (2025)

Ariens Snow Throwers (Ariens) – Laceration Risk (2025)

Rotarex Atherectomy System (Bard) – catheter breakage (2025)

IntelePACS Software (Intelerad) – image calculation error (2025)

Optima MR360 MRI System (GE Healthcare) – SAR monitoring (2025)

Brivo MR355 MRI System (GE Healthcare) – SAR monitoring (2025)

SIGNA Creator MRI System (GE Healthcare) – SAR monitoring (2025)

SIGNA MR380 MRI System (GE Healthcare) – SAR monitoring (2025)