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All product recalls affecting Missouri.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Missouri in the distribution area.
Firm received multiple complaints of anesthesia circuit leaks due to cracks in the 120" expandable tubing. Cracks and resulting leaks may lead to hypoxia, hypoventilation, and inadequate delivery of inhaled anesthetic agents, which may result in serious injury or death. Volatile anesthetics may also escape into the operating room environment.
Failed Impurities/Degradation Specifications: an out of specification result obtained during routine stability testing for Highest Unknown Impurity .
Failed Impurities/Degradation Specifications: Due to levels of 'Diester Impurity' exceeding the specification limit.
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Failed Dissolution Specifications
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
Failed Impurities/Degradation Specifications: Out of specification for impurity IP-C.
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
This recall involves all Ambiano electric pressure cookers with model numbers 93550 (KY-318B), 96775 (KY-318A), and 98527 (6L-PC). The electric pressure cookers and inner cooker pots are either six-quart or eight-quart capacity. The brand name Ambiano appears on the front of each unit and on its permanent on-product label. The model number of the recalled pressure cookers is also printed on the permanent product label on the bottom of the cooker.
The recall includes the Living Glow five-in-one portable waist fan (model number CP-WFLED01). The model number is found on the label on the back of the fan. The recalled waist fan features five fan speeds, a three-mode flashlight and could be used as a power bank. The recalled fans were sold in gray, white, aqua, coral, red, and sage green. They feature a metal clip for attaching to a belt and a strap for wearing around the neck. The fans measure about 3.6 inches wide by 4 inches tall.
This recall involves Mom Genius Retractable Safety Gates. The safety gate comes in black and gray and has a retractable mesh screen in between metal frames. The gates measure about 33 inches high, with a retractable width up to 118 inches. "Retractable Safety Gate" and model number "SH.20.006B02" are printed on a white label located on the side of the gate.
Autocar, LLC (Autocar) is recalling certain 2024-2026 ACX (Xpeditor) and DC (Legend) vehicles. The tie rod clamp may have been improperly secured.
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
Braun Industries, Inc. (Braun Ambulances) is recalling certain 2023-2026 Chief XL Type I, Express Plus Type I, Liberty Type I, RMT US Type I, and Select Chief XL Type I ambulances. The brake pedal switch may have been damaged, preventing the cruise control from disengaging when the brake is depressed. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard numbers 105, "Hydraulic and Electric Brake Systems" and 124, "Accelerator Control Systems."
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
The impacted lot may not meet the required tensile strength specification.
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
Nissan North America, Inc. (Nissan) is recalling certain 2013-2021 NV200 Van, 2014-2017, 2019 NV200 Taxi, and 2015-2018 Chevrolet City Express vehicles. The Fuel Tank Temperature (FTT) sensor harness may have been incorrectly routed, damaging wires and causing a short circuit in the fuel pump fuse.
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.