State
72,940 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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Nova Bus is recalling certain water pumps because a loose impeller shaft may cause pump failure, increasing crash risk.
About 3,170 Primark Water Balloon Pumps are being recalled because they can generate excessive pressure and rupture. Two US reports of cuts to hands and fingers have been received.
Motorcar Parts of America is recalling specific brake calipers for 2008-2025 Ford E-450 Super Duty vehicles because the piston bore wall may not meet specifications, causing the caliper to fracture.
About 250 FUFU&GAGA queen size Murphy wall beds are being recalled after two reports of the 215-pound frame falling during assembly, injuring two consumers.
About 300 Little Pea Shop padded crib bumpers are being recalled because they can obstruct an infant's breathing and are banned under the Safe Sleep for Babies Act.
About 9,400 CreateOn Crayola-branded pip-Cubes are being recalled because magnets can come loose if the seams separate, posing an ingestion hazard to children.
About 2,300 Grizzly Industrial 15-inch 3HP heavy-duty planers, model G0815, are being recalled because the chip breaker can contact the cutterhead blades and eject debris.
About 4,120 Casaottima 13-Drawer Dressers are being recalled because they are unstable when not anchored to a wall and violate the STURDY Act standard.
About 10,380 KTEBO writing tablet toys are being recalled because the screw securing the button cell battery compartment does not remain attached as the mandatory toy standard requires.
BMW is recalling 2026 X6, X7, X5, and X5 Plug-In Hybrid models. The instrument panel may prevent the passenger-side airbag from deploying properly during a crash.
About 40 Cubimana treehouse building toy sets are being recalled because button cell batteries in the LED light piece can be easily accessed by children.
About 17,000 HydroJug 14-ounce children's sport tumblers are being recalled because the rivets on the handle can come loose, causing the handle to detach and posing a choking hazard.
Fresenius Kabi is recalling 2,199,850 vials of Famotidine Injection USP after out of limit results were obtained for endotoxin testing. The FDA classified it Class I.
Olympus is recalling 7,023 EVIS EXERA III TJF-Q190V duodenovideoscopes after continued reports of positive cultures and infections, and is updating the reprocessing materials.
Medtronic Sofamor Danek is recalling 275,260 Catalyft PL and PL40 expandable interbody spacers because the cage may lose height or collapse, risking migration or neurological injury.
Volkswagen is recalling approximately 629 2023-2024 ID.4 vehicles with defective high-voltage battery cell modules. Misaligned electrodes in the battery may cause fires, posing a risk of injury to vehicle occupants.
Medtronic MiniMed is recalling 12,126 CareLink Clinic installations because a software error displays incorrect data on the 24-hour sensor glucose overview graph.
Stryker is recalling 39,148 NICO Myriad Handpieces because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.
Medical Products Laboratories is recalling 41,328 bottles of Walgreens Saline Nasal Spray with Xylitol over microbial contamination identified as Pseudomonas lactis.
Straumann USA is recalling 61 units of Emdogain because product intended for demonstration purposes only could be placed in patients.
Pivotal Health Solutions is recalling 464 Quantum Intersegmental Tables because damage to the heat function components can lead to overheating, smoldering and melting of the vinyl cushion.
Mindray is recalling 54 Isoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.
Intelerad Medical Systems is recalling 19 IntelePACS InteleConnect and TechPortal installations because a bug can cause data loss in the Relevant Clinical Info field.
Mindray is recalling 148 Sevoflurane V90 Electronic Vaporizers used with the A9 Anesthesia System over the potential for anesthesia leakage.
Stryker is recalling 39,148 NICO Myriad Illumination Packs because tape used to secure components in the packaging contains latex despite the products being labelled latex-free.