stop use immediately Recalls

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

Sanven Technology Recalls VEVOR Garment Steamers for Burn Hazard (2025)

SKCAIHT Mermaid Costumes Recalled for Phthalate Exposure Risk Sold on Amazon (2025)

SKCAIHT recalls Mermaid costumes sold on Amazon after phthalate exposure risk. The recall covers a dress and a matching headband in children’s size XL. Parents should stop using the costumes immediately and request a full refund.

BaoD Recalls Uuoeebb Infant Walkers Sold on Amazon for Fall and Entrapment Hazards (2025)

Primark Recalls Little Bear 2-Pack Soother Clips Over Choking and Laceration Hazards (2025)

Luyuan Recalls X-Pro Eagle 40cc Youth ATV and FRP Sahara 40cc Youth ATV for Crash Hazard (2025)

GE HealthCare Recalls Nuclear Medicine Systems Over Fall Risk

Mazor Robotics Recalls Robotic Guidance System Over Software Errors

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

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.

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.

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.

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.

GE HealthCare Recalls Nuclear Medicine Systems Due to Fall Risk

Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage

Heraeus Medical GmbH recalled PALACOS R pro 40 and R pro 80 bone cement on December 9, 2025. The recall follows multiple complaints of ampoule breakage affecting product usability. Healthcare providers must stop using the product immediately.

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.

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

Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard

Hyundai IONIQ 6 Recall Expands for Charging Port Door Detachment

Hyundai Motor America recalls 2023-2025 IONIQ 6 electric vehicles due to a charging port door panel that may detach. Dealers will apply adhesive as the remedy. Owner letters begin November 10, 2025. VINs searchable on NHTSA as of September 13, 2025.

Heraeus Medical Recalls PALACOS Bone Cement Due to Ampoule Breakage Hazard

Heraeus Medical GmbH recalled PALACOS MV pro 40 and MV pro 80 bone cement on December 9, 2025. The recall follows numerous complaints about ampoule breakage. This defect can prevent proper cement dough formation, rendering the product unusable for patients.