State
73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Suzuki is recalling 2012-2013 SX4 vehicles because the power steering pump may seize, causing loss of steering assist and increasing crash risk.
Newmar is recalling specific Dutch Star, Dutch Aire, and King Aire motorhomes because a flexible exhaust tube may tear, allowing hot exhaust to contact other components and increase fire risk.
Michelin is recalling specific X Works XZY tires because they lack required DOT symbols and load range letters, which may cause confusion with non-compliant tires.
Eaton is recalling specific FR-Series 10-speed manual transmissions because the reverse gear may stay engaged, causing the vehicle to move backwards unexpectedly.
Henderson Wheel is recalling torsion arm assemblies where the arm is too small for its housing, posing a risk of trailer detachment and loss of control.
Motor Coach Industries is recalling 145 model year 2015 D4000, D4005, D4500, and D4505 vehicles because an incorrectly assembled fuse block may cause arcing and increase the risk of a fire.
Winnebago is recalling 172 model year 2015-2016 Itasca Sunova and Winnebago Sightseer motorhomes because a wiring harness may be damaged, increasing the risk of fire.
Mitsubishi is recalling 2011 Outlander Sport vehicles manufactured on December 3, 2010, due to incorrect certification labels lacking the correct VIN. Dealers will install corrected labels free of charge.
Toyota is recalling 2009-2012 RAV4 and 2012-2014 RAV4 EV vehicles because water dripping on the wiper joint may cause corrosion and linkage separation, reducing visibility.
Triple E is recalling 2016 Libero and Serenity recreational vehicles because a screw may become electrically charged, posing a shock hazard.
Bed Handles Inc. is recalling about 113,000 portable bed handles that lack safety retention straps. The missing straps allow the handles to shift, creating gaps that pose a risk of entrapment, strangulation, and death.
The Land of Nod is recalling Follow the Herd mobiles because unraveling yarn poses an entanglement and strangulation risk to young children.
Zak Designs is recalling 26-ounce water bottles sold at Target because the inner plastic straw can break, posing a choking hazard. No injuries have been reported.
USDA FSIS issued a public health alert for frozen, raw, stuffed chicken products from Aspen Foods due to confirmed Salmonella Enteritidis contamination.
Di Stefano Cheese Co. is recalling approximately 1,280 pounds of Parma Boneless Ham produced in Italy that were not presented for U.S. inspection.
Insulet Corporation is recalling specific OmniPod insulin devices because they may fail to deploy or retract the cannula, potentially disrupting insulin delivery.
Intuitive Surgical is recalling 6,309 Fundus Graspers used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.
Insulet Corporation is recalling specific OmniPod insulin devices because the cannula may fail to deploy or retract, potentially interrupting insulin delivery.
Forest River is recalling 2011-2016 Coachmen Pursuit, Mirada, and Encounter motorhomes because trailer hitch bolts may not be properly tightened, risking hitch detachment.
Intuitive Surgical is recalling 8,217 Maryland Dissector instruments used with the da Vinci Si Surgical System because the jaws may become fixed in a closed position.
Intuitive Surgical is recalling Cadiere Forceps used with the da Vinci Si Surgical System because the instrument jaws may become fixed in a closed position.
Terumo is recalling 4,638 CDI 500 Blood Parameter Monitoring Systems worldwide due to inaccurate readings of vital blood parameters following a software upgrade to version 1.69.
3M is recalling DuraPrep Surgical Solution because the product may be contaminated with a toxic compound.
Smith & Nephew is recalling specific Birmingham Hip Resurfacing Acetabular Cups because the system's revision rates were higher than established benchmarks.
Medtronic Perfusion Systems is recalling Hemocor Hemoconcentrators because they demonstrate low ultrafiltration performance below product specifications.