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.
Ningbo Litesun Electric is recalling about 42,000 outlet converters sold at Home Depot due to reverse polarity, which poses shock and fire hazards.
Cost Plus World Market is recalling Girona outdoor dining chairs because the seat base can separate from the back, causing the chair to collapse and posing a fall hazard.
Forest River is recalling 2018 Puma recreational trailers because wheel center caps may prevent proper tightening, increasing the risk of wheels detaching.
Wabash National is recalling 2018 Van trailers because brake caliper bolts may not be properly torqued, risking caliper detachment and loss of braking ability.
Harbor Freight is recalling specific Innova and Far East utility trailer tires that may not be strong enough to support expected loads, increasing crash risk.
Thor Motor Coach is recalling 2017-2018 motorhomes because incorrect water capacity labels may lead to vehicle overloading and increased crash risk.
E-One is recalling 2016-2017 Quest, Typhoon, and Cyclone II emergency vehicles because the power steering assist cylinder may not be properly tightened, increasing crash risk.
Harbor Freight is recalling 2014-2017 Haul Master trailers because the tires may not be strong enough to support expected loads, increasing crash risk.
Daimler Trucks North America is recalling 2017-2018 Freightliner Cascadia vehicles because the upper steering pinch bolt may not be properly tightened, risking loss of steering control.
Keystone RV is recalling 2018 Crossroads Cruiser and Volante trailers because they may have propane detectors instead of required carbon monoxide detectors.
Daimler Trucks is recalling 2016 Western Star 4900 and Freightliner Cascadia trucks because a steering component may loosen, potentially causing a loss of steering control.
Subaru is recalling 9,178 2015 WRX vehicles because trunk items may cause subwoofer wiring to short, potentially leading to overheating and fire.
John Evans is recalling 2017-2018 Flatbed trailers because air brake diaphragms may degrade, causing emergency brakes to engage and increasing crash risk.
Forest River is recalling 2014-2017 Berkshire XL and XLT buses because headlights may shut off when switching beams, increasing crash risk.
Mercedes-Benz is recalling 495,290 vehicles because the driver's air bag may deploy unexpectedly due to insufficient grounding, increasing injury risk.
Cheetah Chassis Corporation is recalling specific 2017-2018 trailer chassis models because air brake diaphragms may degrade, causing emergency brakes to engage unexpectedly.
Volkswagen Group of America is recalling 216,913 Audi A5, A4 Allroad, and Q5 vehicles because contact corrosion in the auxiliary heater connector may cause wires to overheat or melt, increasing the risk of a fire.
General Motors is recalling 2015-2016 Chevrolet Colorado, GMC Canyon, and 2016 Chevrolet Volt vehicles because the driver's frontal air bag may inflate improperly during a high-speed crash.
Toys R Us is recalling Bruin infant wiggle balls because rubber knobs and plastic parts can detach, posing a choking hazard to infants.
Zimmer Biomet is recalling 4,423 ECT Internal Fracture Fixation Drills because raw material anomalies may increase the risk of instrument fracture during use.
Zimmer Biomet is recalling 1,129 orthopedic surgical drills and screw taps due to raw material anomalies that may increase the risk of instrument fracture.
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may cause the instruments to fracture during use.
Zimmer Biomet is recalling specific orthopedic surgical instruments due to a raw material anomaly that may increase the risk of instrument fracture during use.
Pfizer is recalling 18,725 vials of Sterile Water for Injection due to cracked or chipped glass at the neck, which poses a non-sterility risk.
Zimmer Biomet is recalling specific orthopedic drill bits and screw taps because raw material anomalies may increase the risk of instrument fracture during use.