1,862 recalls tagged with “stop use immediately”.
Medline Industries recalled 236 medical procedure kits on December 12, 2025. The kits contain MASTISOL liquid adhesive that may cause butyrate tubing to crack. Patients and healthcare providers should stop using these kits immediately.
Medline Industries recalled select medical procedure convenience kits on December 12, 2025. The recall affects 40 units due to risks associated with MASTISOL liquid adhesive. The adhesive's tubing may crack during use, posing safety concerns.
Medline Industries, LP recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive linked to cracking tubing during use. Healthcare providers and patients must stop using these kits immediately.
Medline Industries recalled 1,928 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive, which has defective butyrate tubing. Cracking during use poses a high risk to patients and healthcare providers.
Medline recalled 96 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive with defective tubing that can crack during use. Patients and healthcare providers should stop using these products immediately.
Philips recalled 10,466 Azurion Systems on December 12, 2025, due to six software issues that can cause system failures. Users must stop using the devices immediately. The recall affects models sold worldwide, including in the U.S.
Medline Industries recalled 1,928 medical procedure convenience kits on December 12, 2025, due to a risk of crack in the adhesive tubing. The kits contain MASTISOL liquid adhesive, leading to safety concerns. Healthcare providers and patients should stop using the kits immediately and follow the recall instructions.
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.
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.
Sanven Technology recalled Vevor ice crushers on December 11, 2025, due to a fire hazard. The recall affects models BY-300 and BY-300 FS, which can ignite during use. Consumers must stop using these products and seek a refund immediately.
TREK recalled Model Year 2026 electric bicycles on December 11, 2025. The recall affects Domane+ ALR 5, Domane+ ALR 6 AXS, Checkpoint+ SL 6, and Checkpoint+ SL 7 models. Loose chainring bolts may cause falls or crashes, posing a risk to users.
SKCAIHT recalled children's mermaid costumes on December 11 due to a risk of injury from phthalate exposure. The costumes, sold on Amazon, violate federal regulations concerning toxic substances. Consumers should stop using the costumes immediately and seek a 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.
BenTalk recalled YCXXKJ-branded baby bath seats on December 11, 2025. The recall affects models that violate safety standards and pose a drowning risk. Consumers should stop using the product immediately and seek a refund.
Luyuan recalled X-Pro Eagle 40cc and FRP Sahara 40cc Youth ATVs on December 11, 2025. The ATVs violate mandatory safety standards and pose serious injury risks. Consumers must stop using the ATVs and contact Luyuan for a free repair.
Uuoeebb recalled infant walkers on December 11, 2025 due to fall and entrapment hazards. The recall affects collapsible walkers with eight wheels and adjustable heights. Consumers should stop using the product immediately and seek a refund.
Sanven Technology recalled VEVOR Garment Steamers on December 11, 2025, due to burn hazards. Users reported risks of leaking hot water and steam. Consumers should stop using the product and seek refunds immediately.
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.