State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
LCB Manufacturing is recalling 2017-2018 Pitbull roll-off trailers because brake caliper bolts may not be properly torqued, which could cause the caliper to detach and result in a loss of braking ability.
Macy's is recalling Martha Stewart Whiteware cake knife and server sets because the ceramic handles can break, posing a laceration hazard.
Zhaoqing Junhong Co., Ltd. is recalling specific Antares Comfort A5 tires because they may experience sidewall separation while driving, increasing the risk of a crash.
West-Mark is recalling one 2011 tanker trailer because brake caliper bolts may not be properly torqued, which could cause the calipers to detach and result in a loss of braking ability.
Keystone RV is recalling 2018 Carbon, Fuzion, and Raptor triple axle toy haulers because an incorrectly welded suspension equalizer may fail, increasing crash risk.
KZRV is recalling 2017-2018 Sportsmen Sportster trailers because the slide-out support arm may contact the tires, potentially damaging them and increasing crash risk.
HME is recalling 2015 Silverfox SFO fire emergency trucks because improperly torqued steer axles may cause the tie rod to loosen, leading to a loss of steering.
Polaris is recalling 2010-2017 Victory motorcycles because engine misfires can melt the rear brake line, increasing crash risk.
Tesla is recalling 2016-2017 Model X vehicles because the left-side second-row seat backs may not fully latch, increasing injury risk in a crash.
Triple E RV is recalling 2016-2018 Wonder motorhomes because the fridge power supply is not correctly fused, increasing the risk of fire.
Garden of Life is recalling 8,475 units of Baby Organic Liquid probiotic formula due to a choking hazard for newborns caused by the liquid's thickness.
Caterpillar is recalling 2016 CT660 trucks because a loose tie rod could cause a complete loss of steering, increasing crash risk.
Inopak Ltd is recalling Option Systems and STYLE Antibacterial Hand Wash due to GMP deviations and potential bacterial contamination from a pump.
Nissan is recalling 2012 Versa Hatchbacks sold in 23 states and D.C. because road salt may corrode front coil springs, potentially causing them to fracture and puncture tires.
Pro Bioteks Laboratories is recalling Bio-35 dietary supplements because they contain undeclared soy lecithin, a common allergen.
KIND LLC is recalling Dark Chocolate Nuts and Sea Salt Bars because the outer box fails to declare the allergen walnuts, although individual bars are properly labeled.
Permobil is recalling 146 electric wheelchair bases due to a potential failure of the top plate assembly that connects the seating system to the base.
Permobil is recalling 5,539 Corpus II electric wheelchairs because the top plate assembly may fail, potentially disconnecting the seating system from the base.
Radiometer America is recalling AutoCheck5+ Level 2 quality control ampoules because they may provide incorrect pCO2 and pO2 results.
Inopak Ltd is recalling Choice Antibacterial Hand Soap due to GMP deviations and potential bacterial contamination from a pump.
Implant Direct is recalling 50 units of Swish Duo-Grip Healing Collars because the packages contained the wrong component size.
Inopak Ltd is recalling specific batches of Mild Healthcare Antibacterial Hand Soap due to potential bacterial contamination from a defective pump.
Carl Zeiss Meditec AG is recalling nine INTRABEAM PRS 500 radiation therapy devices because they had incorrect printed calibration values on their certificates.
Pfizer is recalling 32,276 vials of Deferoxamine Mesylate for injection due to a failure to control impurities causing color change at the API stage.
Chrysler is recalling specific 2012-2013 vehicles because a component failure may prevent active headrests from deploying in rear-end crashes, increasing injury risk.