State
73,104 recalls have nationwide distribution and so reach Vermont. 2,009 additional recalls listed Vermont specifically in their distribution scope.
Of the 2,009 recalls naming Vermont we have scored against our rubric, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 419 (21%) are Severe.
Which agencies issued them
These figures cover only the 2,009 recalls whose distribution notice names Vermont specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lupin Pharmaceuticals is recalling one lot of Cefixime oral suspension (200 mg/5 mL) due to failed content uniformity specifications. The recall affects 3,552 bottles distributed nationwide.
Beaver Visitec International is recalling the Xstar Safety Slit Knife Model 378227 because some units have the blade bevel installed incorrectly—facing downward instead of the intended upward orientation.
Howmedica is recalling the Gray Revision Instrument System Accessory Tray/Case due to a design flaw that may enable reuse and re-sterilization of single-use, sterile-packaged instruments.
Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.
Consumer Product Partners is recalling Pure Petroleum white petrolatum products sold at Rite Aid, Kroger, Harris Teeter, and CVS nationwide because the products labeled as pure white petrolatum actually contain undisclosed lavender and chamomile.
Baxter Healthcare is recalling Centrella Max and Pro+ hospital bed mattresses that may develop delaminated top covers when cleaned with bleach-containing solutions. The mattresses prevent and treat pressure injuries.
Polestar is recalling certain 2021-2024 Polestar 2 vehicles because Infotainment Head Unit software may prevent the rearview camera image from displaying, failing FMVSS 111.
Howmedica Osteonics Corp. is recalling HRIS Storage & Sterilization Cases (Part 6210-9-900) due to a design flaw that may allow reuse and resterilization of single-use, sterile instruments. This poses a contamination and infection risk.
NxStage PureFlow-B hemodialysis solution bags may burst during preparation, releasing caustic electrolyte fluid that can cause chemical burns. Affected units are distributed nationwide.
Ethicon is recalling VICRYL Plus Antibacterial Sutures due to a packaging machine defect that created holes in the primary packaging, potentially compromising product sterility. Affected sutures may pose an infection risk.
Ethicon recalls 306,000 MONOCRYL surgical sutures worldwide due to holes in primary packaging from a manufacturing defect that compromises sterility and could result in infection.
Ethicon recalls PDS Plus Antibacterial sutures due to packaging defects that compromised sterility. The affected units may cause infection if used in surgery.
Eugia US LLC recalls 70,125 vials of Dexamethasone Sodium Phosphate injection due to failed impurity specifications. Testing found sulfonic acid adduct of dexamethasone phosphate exceeded allowed limits.
Beaver Visitec International is recalling 126 Xstar Safety Slit Knives with incorrect blade configuration. The recalled knives have the bevel oriented to the back instead of the front.
Eugia US LLC is recalling 15,500 vials of Eptifibatide injection nationwide due to failed impurities and degradation specifications. The defect involves a related substance identified as Eptifibatide dimer.
SEA Electric is recalling 174 vehicles because a software defect may cause the high-voltage battery to shut down, resulting in a loss of drive power.
FCA US is recalling 2014-2019 Fiat 500 vehicles because the tire pressure warning light may fail to illuminate, increasing crash risk.
MGA Entertainment recalls about 21 million Miniverse Make It Mini Sets with unused liquid resins due to risk of skin, eye, and respiratory irritation. The recalled sets contain acrylates in amounts prohibited in children's products.
Brinkley RV is recalling certain 2023-2024 Model Z fifth wheels and Model Z-Air travel trailers because the 12-volt refrigerator wiring may overheat. 3,157 units affected.
SEA Electric is recalling certain electric vehicles because a software defect in the battery management system can cause a loss of drive power, increasing crash risk.
Jaguar is recalling certain 2021-2024 F-Pace vehicles because the oil filter housing can crack and leak oil into the engine compartment. 150 units are affected.
Oshkosh is recalling 2025 Defense NGDV ICE vehicles because deformed wiring harness terminals may prevent air bags from deploying as intended.
Bigfoot is recalling 2023-2024 B25RQ travel trailers because a faulty LED circuit board may overheat and cause a fire.
Isuzu is recalling 2025 FTR vehicles because incorrectly heat-treated ball studs in the tie rod assemblies may break, potentially causing loss of steering control.
Nissan is recalling specific INFINITI models because the driveshaft can fatigue and break, potentially causing loss of drive power or vehicle roll-away.