2,229 recalls tagged with “stop use immediately”.
Sysmex America recalled 44 units of the TS-10/TS-10H Tube Sorter on December 15, 2025. The electromagnetic holding force may disengage, causing unintended movement. Healthcare providers should stop using the device immediately.
Philips Medical Systems recalled four Allura Xper FD20/10 systems on December 15, 2025. The company identified that a drip tray was not installed, posing a risk of electrical shorts. This defect could lead to system shutdowns.
Philips Medical Systems recalled 23 units of the Allura Xper FD20 Biplane on December 15, 2025. The recall affects systems with improperly installed drip trays, posing an electrical hazard. Health providers and patients must stop using the device immediately.
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Wilson-Cook Medical recalled 60 units of Nasal Jejunal Feeding Tube NJFT-10 on December 15, 2025. The tubes were packaged without the necessary nasal transfer tube component. This defect poses a high hazard risk for patients requiring feeding assistance.
Product contains potentially harmful dosing errors for Vecuronium, Flumazenil, and Ketamine.
Elekta recalled 5,391 medical linear accelerators on December 14, 2025. A manufacturing issue related to electrical grounding poses a serious hazard. Patients and healthcare providers must stop using these devices immediately.
It was found that the MX40 device could not reconnect to the PIC iX when moving between Radiohead and Trident 1.4 GHz access points if the signal strength changed quickly.
Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that is included in the Microsensor and Cerelink ICP Kits.
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.
Potential contamination with biological hazards (Listeria monocytogenes).
due to a defect associated with the conductivity values of the solution used to calibrate meters and result in the reporting of incorrect conductivity values for dialysate.
Presence of particulate matter: potential presence of metal particulates in the product.
Presence of particulate matter: potential presence of metal particulates in the product.
Medline Industries recalled 60 medical procedure convenience kits on December 12, 2025. The kits contain MASTISOL liquid adhesive which has a defect causing butyrate tubing to crack. Users must stop using the kits immediately and follow recall instructions.
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.