State
72,984 recalls have nationwide distribution and so reach Vermont. 1,983 additional recalls listed Vermont specifically in their distribution scope.
Of the 1,983 recalls naming Vermont we have scored against our rubric, 199 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 409 (21%) are Severe.
Which agencies issued them
These figures cover only the 1,983 recalls whose distribution notice names Vermont specifically. The 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Glenmark Pharmaceuticals is recalling approximately 58,416 bottles of Atomoxetine 80 mg capsules nationwide due to the presence of N-Nitroso Atomoxetine impurity above FDA-recommended limits. This is a Class II recall.
Glenmark Pharmaceuticals is recalling Atomoxetine 25 mg capsules nationwide due to the presence of N-Nitroso Atomoxetine impurity above FDA-recommended limits. Approximately 175,920 bottles are affected.
Dexcom G6 continuous glucose monitors may fail to deliver high or low blood sugar alarms due to a software error, potentially delaying detection of dangerous glucose levels. Alarms will be delayed and skip in sequence until the device is reset.
Glenmark Pharmaceuticals is recalling Atomoxetine capsules due to N-Nitroso impurity levels exceeding FDA recommended limits. The recall affects 56,208 bottles nationwide with specific lot numbers.
Hollister is recalling AnchorFast Guard endotracheal tube fasteners because decreased skin barrier wear time could cause tube migration. The recall affects multiple lot numbers distributed in the US and Canada.
RayStation radiation therapy planning software contains an inconsistency in density uncertainty calculations within dose planning functions affecting proton and light ion treatments in versions 4.5 through 2024B.
XTANT Medical Holdings is recalling Irix-A Lumbar Fusion System implants due to incorrect expiration date labeling on sterile spacers. Fourteen units were distributed in Arizona, California, Colorado, Louisiana, Ohio, Texas, West Virginia, and Australia.
AvKARE is recalling Silodosin 8mg capsules nationwide due to subpotent drug levels and out-of-specification impurity found in stability testing. The affected lot is BC20223A, expiring March 31, 2025.
Glenmark Pharmaceuticals is recalling 120,000 bottles of Atomoxetine 10 mg capsules nationwide due to N-nitroso Atomoxetine impurity exceeding FDA recommended limits. Multiple lot numbers are affected with expiration dates through July 2026.
Mercedes-Benz is recalling 2021-2023 S-Class and Maybach vehicles because front brake hoses may rupture and leak fluid, increasing stopping distance and crash risk.
Kawasaki is recalling 2024 Ninja e-1 and Z e-1 motorcycles because a missing battery terminal anchor may cause loss of drive power, increasing crash risk.
Kia is recalling certain 2025 EV9 vehicles because the rear gear drive unit motor shaft may have been improperly welded and become damaged, causing a loss of drive power.
Grand Design is recalling 2025 Serenova travel trailers because improperly tightened axle bearing nuts may cause overheating, increasing the risk of fire or tire detachment.
Joyson is recalling one side curtain air bag inflator because the ignition holder may detach during deployment, creating a projectile hazard.
Textron is recalling 2024-2025 Cushman and E-Z-GO low-speed vehicles because side and rear reflectors do not meet federal safety standards, increasing crash risk.
LPK1 is recalling ready-to-eat chicken Caesar wraps because the included dressing contains undeclared fish (anchovies). No adverse reactions have been reported.
BMW is recalling certain 2025 X3 30 xDrive vehicles because the connection between the positive battery cable and the starter-generator may be improperly tightened and overheat.
Forest River is recalling 2025 Coachmen Catalina travel trailers because the towing coupler may be underrated for the trailer's weight, posing a crash risk.
Shyft Group is recalling certain 2022-2025 Spartan RV Chassis K2 vehicles with Cummins L9 diesel engines because the remote fuel filter hose may separate from the fitting.
Forest River Bus is recalling 2024 Starcraft Allstar Transit buses because the emergency exit window handle may not be visible from the aisle, potentially delaying evacuation.
Keystone is recalling 2024-2025 Outback 330RL travel trailers because a side window was incorrectly labeled as an emergency exit, which could delay evacuation.
Forest River is recalling certain 2017-2025 Coachmen Catalina, 2020-2025 Aurora and 2025 Puma travel trailers because the Gross Vehicle Weight Rating on the Federal placard may exceed the safety chain rating.
Walmart recalls about 17,970 Swagtron SG-5 Boost electric scooters due to lithium-ion batteries that can overheat, smoke, and ignite, causing fire and burn hazards. One incident caused a burn injury and property damage to a residential building.
BMW is recalling certain 2022-2024 X3 sDrive30i and xDrive30i vehicles because second-row door locking modules may allow the doors to be unlocked with a single motion, failing FMVSS 206.
Honda is recalling certain 2024 CB650R and CBR650R motorcycles because the gear shift arm fasteners may loosen and detach, leaving the rider unable to change gear.