State
73,833 recalls have nationwide distribution and so reach Rhode Island. 3,054 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,054 recalls naming Rhode Island we have scored against our rubric, 221 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 708 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,054 recalls whose distribution notice names Rhode Island specifically. The 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Tiffin Motorhomes is recalling 2014 Breeze motorhomes because a steering knuckle may fracture, potentially causing loss of vehicle control and increasing crash risk.
Haldex is recalling specific air brake actuators where an internal defect may cause brake drag and overheating, increasing the risk of fire.
Rapala is recalling StrikeMaster Lithium Lazer ice augers because the trigger switch may fail to turn off the unit, posing an injury risk.
Forest River is recalling one 2015 XLR Hyperlite trailer because fuel vapors may ignite near a fuel-burning appliance. The unit is being repaired at the dealership before delivery.
PACCAR is recalling 2006-2016 Peterbilt trucks because tire labels may list incorrect pressure, risking tire failure and crashes.
Multiprens is recalling STK-100 triangle kits manufactured between October 2011 and July 2014 because they fail to meet Federal Motor Vehicle Safety Standard No. 125.
Sugar Daddy LTD is recalling 1,000 Caramel Apples because CDC epidemiologists linked a Listeria monocytogenes illness outbreak to the product.
Sugar Daddy LTD is recalling caramel apples linked to a Listeria monocytogenes outbreak. Consumers should not eat the product.
Invacare is recalling 1,942 TDX, FDX, and Storm Series power wheelchairs because wire pinching can cause smoking, sparking, or fire.
Hospira is recalling 190 Plum A+ infusion pumps because their alarm assemblies may fail to sound at any volume level.
HeartWare Inc is recalling 4,845 HeartWare Controllers used in ventricular assist systems because they are more susceptible to electrostatic discharge (ESD) than newer models.
Invacare is recalling 60 FDX, TDX, and Storm Series power wheelchairs because wire damage can cause smoking, sparking, or fire.
Invacare is recalling 525 electric wheelchairs because a seating defect can pinch wires, potentially causing smoking, sparking, or fire.
Hospira is recalling 4,656 Plum A+ infusion pumps because one lot of alarm assemblies may fail to sound at any volume level.
Hospira is recalling 3,939 Plum A+ infusion pumps because one lot of alarm assemblies may fail to sound at any volume level.
Hospira is recalling nine Plum A+ infusion pumps because their alarm assemblies may fail to sound at any volume level.
Daimler Trucks North America is recalling 2007-2011 Freightliner Cascadia trucks because water leaks may cause electrical shorts, leading to trailer light failures or fires.
Par Pharmaceutical Inc. is recalling Mafenide Acetate 5% Topical Solution packets due to the presence of oxidized steel, organic material, and shredded polypropylene.
Hospira Inc. is recalling 315 Plum A+ infusion pumps because one lot of alarm assemblies may fail to sound at all volume levels.
NABI is recalling 63 model year 2014 40LFW city transit buses because improperly torqued tie rod nuts may cause loss of vehicle control and increase crash risk.
Navilyst Medical is recalling NAMIC Convenience Kits because expiration dating is not fully supported by shelf life testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 13 units of NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 512 NAMIC Convenience Kits because expiration dating is not fully supported by testing, posing a potential sterility breach and infection risk.
Navilyst Medical is recalling 541 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased infection risk.
Navilyst Medical is recalling 10 NAMIC Convenience Kits because expiration dating is not fully supported by testing, which may result in a sterility breach and increased risk of infection.