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All product recalls affecting Kentucky.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Kentucky in the distribution area.
During the assembly of Prodisc C, a blue discoloration was observed on a Prodisc C inlay. The discoloration is considered a foreign contaminate that may not have been fully evaluated in the manufacturing validations.
Uncertainty in the seal integrity of the sterile packaging.
Uncertainty in the seal integrity of the sterile packaging.
There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
This recall involves the Manhattan Toy Brilliant Bee Rattle. The toy has a plastic light-up bee attached to a wooden rod and wooden base. There are three plastic rings on the rod and a baby-safe mirror on the bottom of the base. The bee rattle has non-removable batteries, and the model number "166700 CQ" is printed on the base. The toy measures about seven inches tall and four inches wide.
Winnebago Industries, Inc. (Winnebago) is recalling certain 2021-2025 Ekko motorhomes. The solar charging system was incorrectly designed without sufficient over-current protection, which can allow the circuit to overheat and melt the fuse.
This recall involves multiple models of the BISSELL Steam Shot Handheld Steam Cleaners in the model series 39N7 and 2994. "STEAM SHOT" or "POWER STEAMER" is printed on the side of the product. The model numbers are printed on the product rating label located on the bottom of the unit. Colors include green, pink, blue, orange, white, black, purple and red.
Chrysler (FCA US, LLC) is recalling certain 2017-2018 Pacifica Plug-In Hybrid Electric (PHEV) vehicles that received a software update remedy under NHTSA recall number 22V-077. The battery pack may cause a vehicle fire when parked, even with the ignition in the "Off" position.
There is the potential for holes in the clear sterile barrier of the device pouch which may impact device sterility.
This recall involves 2022-2023 CFMOTO ZFORCE 950 HO Sport Side-by-Side Recreational Off Highway Vehicles sold in gray, orange, and tan colors. CFMOTO is stamped on the front of the vehicle and ZFORCE is printed on the side of the chassis. The VIN is stamped on the vehicle's frame, just ahead of the right rear wheel.
Defective container; yellow colored spike from cap lodged in the nozzle
Marketed without Approved NDA/ANDA. FDA analysis found product to be tainted with undeclared Diclofenac and Omeprazole.
Hyundai Motor America (Hyundai) is recalling certain 2023 Xcient vehicles. The pitman arm may not be secured properly to the steering gearbox, which can result in a loss of steering control.
Uncertainty in the seal integrity of the sterile packaging.
Software anomalies which can result in two separate issues: A lagging screen display during a navigated procedure; or the potential for a mismatch between the navigated screw and the screw information presented on the screen.
BMW of North America, LLC (BMW) is recalling certain 2018-2023 X3 sDrive30i, X3 xDrive30i, X3 M40i, and X3 M vehicles. The attachment for the interior cargo rail may become damaged in a rear crash and result in the cargo rail detaching.
Suzuki Motor USA, LLC (Suzuki) is recalling certain 2023-2024 DL800DE motorcycles. The rear tire may crack or deform, resulting in tire tread separation.
The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.
The adhesive joint between the plastic socket and metal component of the Power Express Sample Holder can fail, causing the metal part to detach and enter the centrifuge. This detachment can result in damage to the centrifuge and potential destruction of the patient sample resulting in delayed results and possible exposure of lab technician to biohazardous material.