2,153 recalls tagged with “stop use immediately”.
NIPRO Technical Services recalled 499 units of Conductivity Standard Solutions on December 12, 2025. A defect affects the conductivity values, leading to incorrect readings for dialysate. Patients and healthcare providers must stop using the product immediately.
Medline Industries, LP recalled 1,928 circumcision procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which may crack during use. Healthcare providers and patients must stop using these kits immediately.
Medline Industries recalled 456 medical procedure kits on December 12, 2025, due to a potential hazard involving MASTISOL liquid adhesive. The defective butyrate tubing may crack during use, posing a risk to patients and healthcare providers. Consumers must stop using these kits immediately and seek further instructions.
Luyuan recalls two youth ATVs for a crash hazard that could cause serious injury or death. The models are X-Pro Eagle 40cc Youth ATV, CARTOONS, and FRP Sahara 40cc Youth ATV, SHR 40-RED-M. Consumers should stop using the ATVs immediately and contact Luyuan for a free repair.
Primark recalled the Little Bear 2-Pack Soother Clips sold at Primark stores in the Northeast, Florida, Maryland and Illinois from June 2025 through August 2025 for about $5. The wooden button on the clip can detach, exposing a sharp screw. Consumers should stop using the recalled clips and return them to a Primark store for a full refund.
BaoD recalled Uuoeebb Infant Walkers sold on Amazon after safety hazards were identified. The walker can fit through a standard doorway and does not stop at a step edge, creating a fall hazard. The leg openings can allow a child to slip down until the head becomes entrapped. Consumers should stop using the recalled walker immediately and contact BaoD for a full refund.
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.
Sanven Technology recalled VEVOR Garment Steamers sold online after a burn hazard was identified. Affected units can leak or spit hot water, and the water tank cap can leak or detach. Consumers should stop using the recalled steamers and request a full refund from Sanven Technology.
Sanven Technology recalled Vevor ice crushers after a fire hazard was identified in BY-300 and BY-300 FS models. The units, sold as Ice Shavers, Ice Crushers and Snow Cone Makers, can experience a thermal event that could ignite. Stop using the recalled devices immediately and contact Sanven Technology for a full refund.
Applied Medical Resources recalled 450 units of the Kii Low Profile, Bladed Dual Pack on December 11, 2025, due to a potential safety issue. The blade obturator may extend beyond safe limits after assembly, posing a risk to patients. Healthcare providers and patients should stop using the device immediately.
TREK recalled four electric bicycles sold through Trek authorized retailers and independent bike shops nationwide and online. The chainring bolts can loosen, causing the chainring to detach and create a fall hazard. Owners should stop riding immediately and contact an authorized Trek dealer for a free repair; Trek provides a $20 in-store credit toward Trek, Electra, or Bontrager merchandise, valid
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.
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 recalled 148 units of Lumipulse pTau 217 Plasma Controls on December 11, 2025. The recall follows reports of inaccurate test results that misclassify patients regarding Alzheimer’s disease. The affected product may falsely elevate positive or indeterminate results, increasing the risk of incorrect patient classification.
GE HealthCare recalled 12 Nuclear Medicine systems on December 10, 2025, due to a potential fall hazard. The affected systems may have inadequate support during transport, risking detector integrity. No injuries have been reported, but the risk of life-threatening incidents exists.
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 recalled 38 Nuclear Medicine systems on December 10, 2025, due to potential detector falls. The affected systems may have been relocated without adequate support, risking serious injury. No incidents have been reported, but the recall is classified as a Class II hazard.
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 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 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.