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.
Health One Pharmaceuticals is recalling Gamma Zyme dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
Health One Pharmaceuticals is recalling Reishi Mushroom capsules due to significant violations of dietary supplement manufacturing regulations.
Health One Pharmaceuticals is recalling Shu Chang Bao dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
Health One Pharmaceuticals is recalling Motichi dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
Lippert Components is recalling specific trailer axle hubs because wheel mounting studs may fail, potentially causing wheel separation and a crash.
Hino is recalling 2015-2016 238, 258, 268, and 338 trucks because overtightened front axle U-bolts may fail, causing loss of steering.
Keystone RV Company is recalling 2015-2016 Keystone and Dutchmen trailers because wheel studs may break, potentially causing the wheel to detach.
Highland Ridge RV is recalling 238 model year 2015-2016 travel and fifth wheel trailers because slide room screws may fail, allowing the room to extend while driving and increasing crash risk.
PACCAR is recalling 2015-2016 Peterbilt 220 and Kenworth K300 trucks because pressing the cruise control decrease button increases speed, increasing crash risk.
BMW is recalling 91,800 MINI Cooper vehicles because the front passenger air bag may not deploy in a crash due to a faulty seat mat.
Autocar is recalling 2013-2015 ACX front-end loader garbage trucks because mounting brackets may fail, causing the cross member to detach and creating road hazards.
General Motors is recalling specific 2004 Buick, Chevrolet, and Pontiac vehicles because a leaking valve cover gasket may cause engine oil to drip onto the exhaust manifold, increasing the risk of a fire.
Bosch is recalling fuel delivery modules with improper nickel plating that may cause the fuel pump to fail, leading to vehicle stalling and increased crash risk.
Forest River is recalling specific 2015-2016 fifth wheel and travel trailers because slide room screws may fail, allowing the room to extend while driving and increasing crash risk.
General Motors is recalling 2014 Chevrolet Impala vehicles because the electronic parking brake may not fully retract, causing excessive heat and potential fire.
Heartland is recalling 2015-2016 fifth wheel and travel trailers because bolts attaching the expanding room may fail, causing the room to extend while driving and increasing crash risk.
PACCAR is recalling 2015-2016 Kenworth T680 and T880 trucks because inadequate axle lubrication may cause bearing failure, increasing the risk of a wheel-end fire or crash.
Nissan is recalling 2014 Rogue vehicles because a fuel pump defect may cause the vehicle to stall without warning, increasing the risk of a crash.
Heartland is recalling 2015 fifth wheel and travel trailers because a rivet on the quad entry steps may shear, causing the steps to fail and increasing the risk of injury.
Volkswagen Group of America is recalling 3,646 2015 Audi Q3 vehicles because the sunroof may continue closing after the vehicle is turned off, posing an injury risk.
Lebanese Butcher Slaughter, Inc. is recalling approximately 902 pounds of beef, goat, and lamb products due to misbranding and lack of full inspection.
Aloha is recalling Vanilla Premium Protein Powder due to the presence of Staphylococcus enterotoxin. The product was sold nationwide online and in New York retail stores.
Baxter Healthcare is recalling 48,874 units of 5% Dextrose Injection because missing closures or leaks may compromise sterility.
Cardiovascular Systems, Inc. is recalling 30 units of the Diamondback 360 Coronary Orbital Atherectomy System because the outer layer may flake off, potentially causing a flow-limiting embolism.
Oshkosh is recalling 2014-2015 S-Series Front Discharge Concrete Mixers because air tanks may hold insufficient volume, increasing crash risk.