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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

567

Class I (Serious)

25

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 521–540 of 7756 recalls

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

1...25 262728 29...388

Page 27 of 388Next

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

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.

Bimatoprost (Aspen Biopharma) – CGMP Deviation (2025)

CGMP Deviations

Class IIModerate

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

Alprostadil (Aspen Biopharma) – CGMP Issues (2025)

CGMP Deviations

Class IIModerate

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

Bodor I Series Laser (Jinan Bodor) – federal standard (2025)

The Bodor i Series products fail to meet certain applicable Federal standards, 21 CFR 1040.10(f)(1) and 21 CFR 1040.10(f)(2).

FDAFeb 7, 2025Nationwide• Jinan Bodor Cnc Machine Co Ltd NO.1299, XINLUO AVE HI-TECH ZONE Jinan China

Bobcat AirFX Mower Deck (Doosan) – Crushing Hazard (2025)

This recall involves Bobcat & Steiner AirFX Finish Mower Deck attachments. The mower decks are all black and labeled with "AirFX" and either "72" or "61" depending on the mower deck model. The following model numbers, located on the rear of the attachment on the right-side frame rail, are included in this recall. Model Number Description 7526575 72" AirFX 7526579 61" AirFX 7449223 61" AirFx Finish Mower 7447341 72" AirFx Finish Mower

CPSCFeb 6, 2025Nationwide• Doosan Bobcat North America, of West Fargo, North Dakota

DxI 9000 Analyzer (Beckman Coulter) – interface board issue (2025)

Beckman Coulter identified that an issue for DxI 9000 tip stocker interface (TSI) and reagent storage interface (RSI) boards with the firmware version 1.1.0.0 can cause sub-system communication failures. This failure could result in a delay in reporting patient results.

FDAFeb 6, 2025Nationwide• Beckman Coulter, Inc.

DxI 9000 Analyzer (Beckman Coulter) – encoder wheel misalignment (2025)

the DxI 9000 encoder wheel was misaligned on the motor shaft, leading to increased slippage errors and causing the instrument to stop, posing a high safety risk due to potential delays in patient results.

FDAFeb 5, 2025Nationwide• Beckman Coulter, Inc.

Spectrum IQ Infusion System (Baxter) – mounting screw issue (2025)

There is the potential for missing motor mounting screws, which may have occurred during the servicing process.

FDAFeb 5, 2025Nationwide• Baxter Healthcare Corporation

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.

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