
immediate action Recalls
2,756 recalls tagged with “immediate action”.


YCXXKJ Baby Bath Seats Recalled for Drowning Risk Sold on Amazon by BenTalk (2025)
YCXXKJ recalled baby bath seats sold on Amazon by BenTalk due to risk of drowning. The seats are unstable and can tip over during use. Stop using the recalled seats and contact BenTalk for a full refund.

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

Primark Recalls Little Bear 2-Pack Soother Clips Over Choking and Laceration Hazards (2025)
Applied Medical Resources Recalls Cannula Due to Blade Hazard
There is the potential for extended length of the blade obturator after assembly into the cannula and seal housing.

TREK Recalls 4 Electric Bicycles Over Chainring Bolt Hazard (2026 Domane+ ALR 5, ALR 6 AXS, Checkpoi
Fujirebio Diagnostics Recalls Plasma Calibrators Over Inaccurate Results
Fujirebio Diagnostics Recalls Lumipulse ¿-Amyloid Controls Over Test Inaccuracy
Fujirebio Diagnostics Recalls Diagnostic Test Over Inaccurate Results
Fujirebio Diagnostics Recalled pTau 217 Plasma Cartridges
Fujirebio Diagnostics Issues Recall for Inaccurate Test Results
Fujirebio Diagnostics Recalls Lumipulse G pTau 217 Plasma Calibrators
Ukrop's Pound Cake Recalled Due to Undeclared Soy Allergen
Ukrop's Homestyle Foods recalled 61 units of its 6" Pound Cake on December 11, 2025. The product contains undeclared soy, posing a risk to those with soy allergies. The cakes were distributed to Virginia and West Virginia.
Instrumentation Laboratory Recalls Coagulation Testing Device Due to Contamination Risk
Instrumentation Laboratory recalled 7,720 coagulation testing devices on December 11, 2025. The recall stems from a potential for microbial contamination. Healthcare providers and patients should stop using the device immediately.
Fujirebio Diagnostics Recalls Lumipulse pTau 217 Plasma Controls Due to High Risk of Inaccurate Test
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.
Mazor Robotics Recalls Robotic Guidance System Over Software Errors
Software errors that can result in incorrect surgical instrument positioning during spinal surgery.
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 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.
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.