State
73,576 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, 209 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 531 (26%) are Severe.
Which agencies issued them
These figures cover only the 2,011 recalls whose distribution notice names Vermont specifically. The 73,576 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Wilton Industries Inc. is voluntarily recalling 1,638 units of Valentine Chip Crunch Sprinkles nationwide due to undeclared milk.
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.
Wilton Industries is recalling Holiday Home Assorted Treat Toppings nationwide due to undeclared milk, a major allergen.
FDA recalls CF Delivery Dev Caps Bravo x5 capsules because they may fail to attach to the esophagus, leading to aspiration.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets because a toxicological assessment found potential for aluminum ions to leach into warmed fluids.
Medtronic is recalling specific Evera and Visia ICD models because a small percentage may experience a shortened Recommended Replacement Time to End of Service interval.
Smisson-Cartledge Biomedical is recalling ThermaCor 1200 Disposable Sets due to a toxicological risk assessment indicating potential aluminum ion leaching into warmed fluids.
Zydus Pharmaceuticals is recalling 1,638 packs of Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
The FDA is recalling Bravo pH Capsule Delivery Devices because the capsule may fail to attach to the esophagus, leading to aspiration and potential hospitalization.
Goal Zero is recalling about 7,850 EC8 power cables because the connector pins can deform and overheat, posing a fire hazard. Four reports of overheating or fire have been received, with no injuries.
Nuts.com is recalling diced dried figs because they contain undeclared almonds, a major food allergen.
Wilton Industries is recalling 18,740 units of Holiday Mix Sprinkles nationwide due to undeclared milk, a major food allergen.
Wilton Industries is recalling Rainbow Chip Crunch Sprinkles nationwide due to undeclared milk, a major food allergen.
CPSC recalls 1.06 million Greenworks and Powerworks pressure washer spray guns because the plastic connector can break, causing impact injuries.
Wilton Industries is recalling 8,742 units of Autumn Assorted Treat Toppings Sprinkles nationwide due to undeclared milk.
Medtronic is recalling specific CRT-D implantable cardioverter defibrillators because a small percentage may experience a shortened time before the device reaches end of service.
CareFusion is recalling BD Alaris Infusion Pump Module Keypads and Door Assembly Kits because fluid ingress can cause unresponsive or stuck keys, potentially delaying medication infusion.
Zydus Pharmaceuticals is recalling Acyclovir Sodium Injection due to customer complaints of crystallization in the finished product.
New Flyer is recalling certain 2013-2021 electric buses because firmware errors in the inverters may cause the electric drive system to shut down, increasing the risk of a crash.
Medtronic is recalling Bio-Console 560 devices because an electrical component may fail, causing the pump to stop and potentially producing smoke or a burning odor.
Utility Trailer is recalling 2006-2021 VS2DC, VS2DX, and VS3DX trailers because a missing weld may cause the slider rail to detach, increasing crash risk.
Nuvasive Specialized Orthopedics is recalling PRECICE STRYDE intramedullary nails due to complaints of adverse events potentially related to biological safety, including pain and bony abnormalities.
Epicure is recalling glass prep bowls that may shatter during use, posing a laceration hazard. Consumers should stop using the product and contact Epicure for a free replacement.
Ferring Pharmaceuticals is recalling 301 ZOMA-Jet 5 Demonstration Kits because the injector pen may break apart and disintegrate into pieces.