State
73,584 recalls have nationwide distribution and so reach Vermont. 2,011 additional recalls listed Vermont specifically in their distribution scope.
Of the 2,011 recalls naming Vermont we have scored against our rubric, 208 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 532 (26%) are Severe.
Which agencies issued them
These figures cover only the 2,011 recalls whose distribution notice names Vermont specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
The Yukon polyaxial screw component in the Yukon Spinal System was recalled because it was incorrectly laser marked with wrong dimensions.
Bausch Health is recalling 895 bottles of Mephyton (phytonadione) 5mg tablets because Impurity D failed stability testing specifications.
Bausch Health is recalling Phytonadione Tablets 5mg because Impurity D exceeded specifications during stability testing. The recall covers 14,089 bottles distributed nationwide.
Sun Pharmaceutical Industries Inc. is recalling Testosterone Cypionate Injection due to an incorrect lot number on secondary packaging.
Shyft Group is recalling 2020-2021 Spartan K2, K3, and K4 RV chassis because steering gear mounting fasteners may come loose, potentially interfering with steering components and increasing crash risk.
Howmet Aerospace is recalling specific Alcoa High Polish Aluminum Wheels that may bend or break under load, increasing the risk of a crash.
Chrysler is recalling certain 2020-2021 RAM 1500 trucks built without a retaining clip securing the brake pedal to the brake system. The missing clip can cause the brake pedal to separate, preventing drivers from applying the brakes and increasing crash risk.
Proterra is recalling 2020-2021 ZX5 vehicles because a front fender flare may splash debris onto the driver's window, impeding visibility and increasing crash risk.
Micro Bird is recalling 2013-2021 G5 school and transit buses because damaged electrical wiring behind the driver's seat may cause a short circuit or fire.
Volkswagen is recalling 2021 Jetta and Tiguan vehicles because bolts may be missing from front seat tracks. Missing bolts allow seats to move freely, increasing the risk of injury in a crash.
Putco is recalling specific Nitro-Lux LED headlamp bulbs because they may cause excessive glare to oncoming drivers, increasing crash risk.
Micro Bird is recalling 2014-2021 G5 School and Transit Buses because damaged electrical wiring behind the driver's seat could cause a short circuit and fire.
Mercedes-Benz is recalling certain 2021 A220, A35 AMG, and CLA250 vehicles because the ISOFIX child seat anchoring bracket on the right-rear seat may be missing the right-side anchoring bar, preventing proper restraint of child car seats.
BMW is recalling certain 2021 X5, X6, and X7 models due to a defect in the steering column shaft universal joint that may not be tightened to specifications, potentially affecting vehicle handling and control.
Tesla is recalling 2012-2018 Model S and 2016-2018 Model X vehicles because center display memory wear can cause loss of rearview camera and turn signals.
Mercedes-Benz is recalling 2019 GLA 250 vehicles because the transmission control unit power supply may interrupt, causing the vehicle to shift into neutral while driving.
Mercedes-Benz is recalling 2017-2021 C300, AMG C43, and AMG C63 vehicles because front seat belts may not fully retract, potentially discouraging use and increasing crash injury risk.
Smeal is recalling 2009-2020 Aerial Fire Apparatus vehicles because a defective trolley can detach from the ladder, posing a risk of injury or death.
Chrysler is recalling certain 2021 Jeep Gladiator vehicles with manual transmissions. The clutch pressure plate may overheat and fracture, increasing the risk of fire and potential loss of drive.
Autocar is recalling certain 2018-2021 Xpeditor vehicles because the seat belt harness may chafe and short circuit the engine, causing unexpected stalling that could lead to crashes.
Penumbra Inc. is recalling 3,368 JET 7 Reperfusion Catheters because the distal tip may become damaged during use, posing a risk of vessel damage and patient injury or death.
Penumbra Inc. is recalling JET 7 Reperfusion Catheters because distal tip damage could cause vessel injury or death during use.
Penumbra Inc. is recalling JET 7 Reperfusion Catheters because distal tip damage could cause vessel injury or death during use.
Penumbra Inc. is recalling JET 7MAX Kits because catheter tip damage during use could cause vessel damage, leading to patient injury or death.
Edge Pharma, LLC is recalling 48 syringes of Ceftazidime Sterile Ophthalmic Solution because the media used for sterility testing was expired, compromising the assurance of sterility.