All Product Recalls

Ukrop's Pound Cakes Recalled Due to Undeclared Soy Risk

Ukrop's Homestyle Foods recalled two pound cake products on December 11, 2025, due to undeclared soy. Consumers with allergies to soy are at risk of serious allergic reactions. A total of 61 cakes were shipped to Virginia and West Virginia.

Fujirebio Diagnostics Recalls Diagnostic Test Over Inaccurate Results

Fujirebio Diagnostics Recalls Plasma Calibrators Over Inaccurate Results

Fujirebio Diagnostics Recalled pTau 217 Plasma Cartridges

Fujirebio Diagnostics Recalls Lumipulse pTau 217 Plasma Controls Due to High Risk of Inaccurate Test

Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Calibrators

GE HealthCare Recalls Nuclear Medicine Systems Due to Fall Risk

GE Healthcare Recalls Nuclear Medicine Systems Due to Fall Hazard

GE Healthcare recalled seven Nuclear Medicine systems on December 10, 2025, due to potential detector falls. The recall affects systems that have exceeded their End of Guaranteed Service. No injuries or falls have been reported.

Phothera 200, Phototherapy Devices indicated for use to treat diagnosed skin disorders such as, but not limited to, Psoriasis, Vitiligo, and Atopic Dermatitis (Eczema) under the direction of a...

Some of the Calibration/Output Certificates had the outputs reversed.

GE HealthCare Recalls Nuclear Medicine Systems Over Fall Risk

White Castle Original Sliders Recalled Due to Undeclared Allergens

White Castle recalled 1,021 cases of Original Sliders on December 10, 2025. The product contains undeclared milk and soy allergens, posing a high risk to consumers. The affected lot codes are 9H203521 and 9H203522, with a Best By date of April 18, 2026.

Publix Coffee Cake Recalled Due to Undeclared Walnuts

Publix recalled 811 cases of Raspberry Coffee Cake on December 10, 2025. The product contains undeclared walnuts, posing a serious allergen risk. Consumers should not consume the product and seek a refund.

GE HealthCare Recalls Nuclear Medicine Systems Over Fall Risk

GE HealthCare recalled three Nuclear Medicine systems on December 10, 2025. The recall follows concerns over inadequate detector support, which could lead to a fall and serious injury. No incidents have been reported to date.

REPLIGEN Spectrometer Recalled Due to Laser Hazard

REPLIGEN Corporation recalled 33 Maverick Measurement Module Spectrometers on December 10, 2025. Disconnected or poorly crimped cables may cause elevated laser output or unintended firing. The recall affects devices distributed in the U.S.

Elekta Recalls MOSAIQ Oncology System Over Overtreatment Risk

Elekta recalled the MOSAIQ Oncology Information System on December 10, 2025. A malfunction may cause overtreatment in patients due to software issues. Healthcare providers should stop using the device immediately and follow recall instructions.

Mazor Robotics Recalls Robotic Guidance System Over Software Errors

Software errors that can result in incorrect surgical instrument positioning during spinal surgery.

Intuitive Surgical da Vinci S/Si EndoWrist Recall 6,152 Instruments for Pitch Cable Frays (2026)

Due to increased in complaints regarding frayed or broken pitch cables on reusable surgical instruments

Intuitive Surgical recalls 2,370 da Vinci S/Si Double Fenestrated Grasper Instruments (2026)

Due to increased complaints for broken/frayed grip cables for reusable instruments.

Intuitive Surgical da Vinci S/Si Monopolar Curved Scissors Recall for 86,904 Units Worldwide (2025)

Due to increased complaints for broken/frayed grip cables for reusable instruments.

Intuitive Surgical da Vinci S/Si Mega Needle Driver Instrument Recall 7,819 Units Worldwide (2026)

Due to increased complaints for broken/frayed grip cables for reusable instruments.