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All product recalls affecting Connecticut.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Connecticut in the distribution area.
The products may contain surface and subsurface contamination of Listeria monocytogenes.
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Zero Motorcycles Inc. (Zero) is recalling certain 2024 DSR/X, DS, DSR, and DSRP motorcycles. The front brake hose may be twisted and become damaged, which can cause a brake fluid leak and a loss of brake pressure.
Ford Motor Company (Ford) is recalling certain 2021-2024 Bronco Sport and 2020-2022 Escape vehicles equipped with 1.5L engines. A fuel injector may crack and leak fuel inside the engine compartment.
Laryngoscope handles may not illuminate as intended.
Unidentified substance of unknown impact was identified on devices during a retrospective evaluation.
Daimler Vans USA, LLC (DVUSA) is recalling certain 2020-2023 Mercedes-Benz Metris vehicles. The electrical connections for the infotainment system may not be properly secured, which can cause the rearview camera image not to display. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility."
Forest River, Inc. (Forest River) is recalling certain 2026 Westbrook and Tracer recreational trailers. The liquid propane (LP) gas hose may be incorrectly routed and rub against the furnace, causing a fuel leak.
Malibu Boats, LLC (Malibu Boats) is recalling certain 2021-2026 Triple Axle Boat Trailers. The brake line may fracture at the connection point to the caliper, causing a loss of brake function.
The products may contain surface and subsurface contamination of Listeria monocytogenes.
CGMP Deviations: The recalling firm filed for Chapter 11 in September 2024. As a result, it cannot monitor the quality program and hence cannot assure that products meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess, rendering the products adulterated.
Laryngoscope handles may not illuminate as intended.
ICU Medical identified two sequences of programming events and alarm interactions that may cause the user interface to become unresponsive.
The products may contain surface and subsurface contamination of Listeria monocytogenes.
Laryngoscope handles may not illuminate as intended.
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.
Devices with firmware versions 2.3 and lower may experience timing variations between software tasks, which could result in skipping the necessary neutral check and the wheelchair producing unintended movement upon power-up when the joystick is out of neutral.