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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

620

Class I (Serious)

91

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 501–520 of 10937 recalls

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

Microstream CO2 Line (Oridion Medical) – Device Usage Risk (2025)

Neonatal-Infant and Adult-Pediatric CO2 Sampling Line/Airway Adapter/CO2 Oral-Nasal Filter Line/Intubated Filter (CO2) Line device users may experience difficulty/inability to disconnect adapter from endotracheal tube for procedures (e.g. suctioning), may cause treatment delay and/or unintended extubation, which could lead to respiratory failure, hypoxia, aspiration, and/or low oxygen saturation.

FDAFeb 17, 2025Nationwide• Oridion Medical 1987 Ltd. Har Hotzvim Industrial

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

Product lacks 510(k) clearance.

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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

Modular Stem (Waldemar Link) – Carton Label Error (2025)

A problem was discovered during the scanning process of the outer carton label because of an incorrect GTIN on the label, which is a GTIN for a different product.

FDAFeb 14, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Milk Chocolate Macadamias (Mauna Loa) – Undeclared Almonds (2025)

Undeclared Allergen

Undeclared almonds

FDAFeb 14, 2025CA, IN, MI• Mauna Loa Macadamia Nut Company, LLC

Potassium Chloride Injection (ICU Medical) – Labeling Error (2025)

Labeling: Label Error on Declared Strength. Cases labeled POTASSIUM CHLORIDE 20 mEq, may contain flexible containers with overwrap mislabeled as 10 mEq. The correct dosage strength of 20 mEq is printed on the labeling affixed to the product flexible container.

FDAFeb 13, 2025Nationwide• ICU Medical, Inc.

Potassium Chloride Injection (ICU Medical) – Labeling Error (2025)

Labeling: Label Error on Declared Strength. Overwrap labeled as Potassium Chloride Inj 10 mEq may contain flexible containers of Potassium Chloride Inj 20 mEq

FDAFeb 13, 2025Nationwide• ICU Medical, Inc.

Alcohol Prep Pads (ViaMed) – Sterility Concerns (2025)

Lack of assurance of sterility and cGMP deviations observed at the manufacturing site.

Class IIModerate

FDAFeb 12, 2025FL• Wuxi Medical lnstrument Factory Co., Ltd.

Synapse PACS Software (Fujifilm) – patient age calculation (2025)

The incorrect computed patient age is showing in VX for patients less than 3 months old.

FDAFeb 11, 2025AZ, AR, CA +27 more• FUJIFILM Healthcare Americas Corporation

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

Sodium Chloride Injection (Nephron) – Potential Leakage (2025)

Lack of Assurance of Sterility: There is a potential for leakage at the IV bottle port.

Class IIModerate

FDAFeb 10, 2025Nationwide• Nephron Sterile Compounding Center LLC

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

C-Section PPS Pack (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

Cysto Pack (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

Ear Pack (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

FDAFeb 6, 2025Nationwide• American Contract Systems Inc

CV Basic Pump Pack (American Contract) – sterilization uncertainty (2025)

ACS is unable to confirm product sterilization assurance requirements were met. Possible loss or lack of functionality may lead to delay or prolonged treatment.

FDAFeb 6, 2025Nationwide• American Contract Systems Inc