EU Safety Gate recall notice for Bouncinette (Babybounce). Reason: The restraint system of the product is not adjustable to the size of the baby. Issued 2022-04
FDA recall notice for Nox T3s Recorder - Product Usage: intended for ambulatory recording of physiological signals during sleep. (NOX MEDICAL). Reason: Error in
EU Safety Gate recall notice for Round Swing with net (Nordic Play). Reason: The knots of the rope may come loose, causing the rope to detach from the seat.…. I
EU Safety Gate recall notice for KN95 mask. Reason: The particle/filter retention of the material is insufficient (measured values:…. Issued 2021-06-04.
EU Safety Gate recall notice for Silicone chain (silikonband). Reason: The soother holder is too long and may lead to strangulation of a child. Issued 2022-10-1
EU Safety Gate recall notice for Lucky Deer Baby Soothing Teether (Dongguan Shiny Industries CO LTD.). Reason: Small part (ball in the foot of the toy) can easi
EU Safety Gate recall notice for Green and Black Liquid Timers Spiral (Playlearn LTD). Reason: The toy may break and the liquid inside may harm the skin of a ch
EU Safety Gate recall notice for Baby Swing (Krea). Reason: The instructions of the product do not state the maximum installation height. Issued 2026-06-12.
EU Safety Gate recall notice for MF8018R-30-6/7-122 (Manuell and Frank). Reason: The product has long functional cords with free ends in the neck area which can
EU Safety Gate recall notice for Grey label hettupeysa (Gray Label). Reason: The product has long functional cords with free ends in the neck area which can…. I
EU Safety Gate recall notice for NK041-06-116 (Nupkeet 1946). Reason: There are long functional cords with free ends in the hood of the product and t…. Issued 2
EU Safety Gate recall notice for Electric Swing BY020 (Emma). Reason: When the seat is in the most reclined position, the swing may tilt close to the…. Issued 2
FDA recall notice for RKN130003, RHEO KNEE 3 YR WARRANTY, MD, CE, External lower limb prosthetic component (Ossur H / F). Reason: Due to firmware issues with th
FDA recall notice for RKNXC0003, RHEO KNEE XC 3 YR WARRANTY, MD, CE, External lower limb prosthetic component (Ossur H / F). Reason: Due to firmware issues with
FDA recall notice for RKNXC0005, RHEO KNEE XC 5 YR WARRANTY, MD, CE, External lower limb prosthetic component (Ossur H / F). Reason: Due to firmware issues with