2,229 recalls tagged with “stop use immediately”.
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
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.
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.
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.
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 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.
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.
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.
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.
Mazor Robotics recalled 549 Mazor X robotic guidance systems on December 10, 2025, due to software errors. These errors may cause incorrect surgical instrument positioning during spinal surgeries. Patients and healthcare providers must stop using the device immediately.
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.
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.
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 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.
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 recalled 86,904 da Vinci S and Si Monopolar Curved Scissors instruments sold worldwide to hospitals and surgical centers. The recall cites increased complaints of broken or frayed grip cables on reusable instruments. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.
Intuitive Surgical recalled 7,819 units of the da Vinci S/Si Mega Needle Driver Instrument sold worldwide to hospitals and healthcare providers. The recall cites broken or frayed grip cables that can impair instrument control. Stop using the device and follow the manufacturer’s recall instructions for replacement or service.
Intuitive Surgical recalled 6,152 da Vinci S, Si Permanent Cautery Hook Instruments distributed to U.S. hospitals and clinics overseas. The defect involves frayed or broken pitch cables. Healthcare facilities should stop using the instruments immediately and follow manufacturer recall instructions. If you operate with these tools, consult your supplier or Intuitive Surgical for next steps.