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All product recalls affecting Vermont.
Includes nationwide recalls (tagged “Nationwide”) and recalls with Vermont in the distribution area.
Due to potential corrosion issues associated with the Backup Battery cable connector that may cause a Backup Battery Fault Alarm.
Labeling: Incorrect or Missing Lot and/or Exp Date
Labeling: Incorrect or Missing Lot and/or Exp Date
The heat function may become damaged over time due to patients pressing on the areas with heat function components. Damage to components can lead to overheating which can lead to smoldering and melting of the vinyl cushion.
Failed Impurities/Degradation Specifications: The result for 'Any individual unspecified impurity' exceeds the specification limit.
CGMP Deviations: N-nitroso-duloxetine impurity above the safety assessment limit of 12.5ppm.
Labeling: Incorrect or Missing Lot and/or Exp Date
The device may either fail to start up, or the transducer may start briefly and then stop, accompanied by an error light on the generator. In addition, the body of the transducer handpiece may gradually increase in temperature during clinical use.
Affected catheters were reprocessed beyond validated cycles. This may compromise device sterility or mechanical integrity of the device and can lead to severe adverse events such as infection, vascular injury or embolism.
Continental Tire the Americas, LLC (CTA) is recalling certain Continental TerrainContact H/T LT265/60R20 121/118R, CrossContact LX25 235/60R18 107V, CrossContact RX ContiSeal 275/40R21 107H, and General Grabber HTS 60LT245/75/R17 121/118S tires. The tires may have been produced using the wrong rubber compound, causing the tread to detach.
BMW of North America, LLC (BMW) is recalling certain 2026 X4 and X6 vehicles. The windshield may not be sealed properly, allowing water to enter the power distribution box or electronic control unit.
BMW of North America, LLC (BMW) is recalling certain 2026 R 1300 RT motorcycles. The cardan shaft may not have been sufficiently hardened, causing the universal joint to slip within the shaft and result in a loss of drive power.
Lack of Assurance of Sterility:
Affected catheters were reprocessed beyond validated cycles. This may compromise device sterility or mechanical integrity of the device and can lead to severe adverse events such as infection, vascular injury or embolism.
Automated cell-locating device barcode reader may read the barcode of the previously processed slide resulting in a misattribution of diagnostic results.
Winnebago Towable (Winnebago) is recalling certain 2025 Access recreational trailers. The shelf above the bed may have been installed incorrectly, which can allow the shelf to detach.
Chrysler (FCA US, LLC) is recalling certain 2020-2025 Alfa Romeo Giulia and Alfa Romeo Stelvio vehicles. The printed circuit board and software for the rearview camera may contain defects that cause the rearview camera image not to display properly. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 111, "Rear Visibility."
Lucid USA, Inc. (Lucid) is recalling certain 2024-2026 Air vehicles equipped with Pure Rear-Wheel Drive. Improperly secured bolts may allow the half-shaft to disconnect from the drive unit.
Lucid USA, Inc. (Lucid) is recalling certain 2022-2025 Air vehicles operating a software version prior to 2.8.0. The lower console display may fail to show a rearview camera image or may show a delayed, inaccurate image of what is behind the vehicle. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 111, "Rear Visibility."
Manufacturing defect causing LCD display issues with missing or partial segments (ghosting) that can result in misreading glucose values, potentially leading to inappropriate treatment decisions for diabetes management.