State
73,597 recalls have nationwide distribution and so reach Rhode Island. 3,048 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,048 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 707 (23%) are Severe.
Which agencies issued them
These figures cover only the 3,048 recalls whose distribution notice names Rhode Island specifically. The 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Navistar is recalling 2021-2022 IC Bus CE school buses because weather seal defects may cause stop sign failures, increasing crash risk.
Honda is recalling 2018-2020 Africa Twin motorcycles because contaminants in the fuel tank may clog the filter, causing engine stalls that increase crash risk.
Honda is recalling certain 2020-2021 Insight, 2020 CR-V Hybrid, and 2020 Accord Hybrid vehicles due to a DC-DC converter fault that may prevent battery recharging, potentially causing loss of drive power and increasing crash risk. Owners can receive a free software update.
Land Rover is recalling 2020 Range Rover Evoque vehicles because the front seat material may burn too quickly in a fire, increasing injury risk.
Ford is recalling certain 2021 E-350 and E-450 vehicles due to mispositioned engine cover insulation that may cause excessive heat and burns to occupants.
USDA FSIS issued a public health alert for Country Meats HOT BBQ Flavor Smoked Pork Snack Sticks due to misbranding and an undeclared milk allergen.
General Motors is recalling 2021 Cadillac Escalade vehicles because the front passenger seat belt and airbag status lights may be invisible in daytime, increasing crash injury risk.
Kanan Enterprises Inc. is recalling On the Go Sweet & Salty Trail Mix because packages contain almonds but do not list them on the label.
Shilpa Medicare Limited is voluntarily recalling 2,064 vials of Busulfan Injection due to CGMP deviations. The recall is nationwide and the lot expired in December 2020.
Veg Pro International Inc. is recalling Fresh Attitude Baby Spinach due to potential Salmonella contamination. The product was distributed across several Northeastern and Mid-Atlantic states.
Volkswagen Group of America is recalling 2020 Audi Q3 vehicles because the brake pedal plate can bend or detach, increasing crash risk.
LG Energy Solution Michigan is recalling about 1,815 RESU 10H home batteries because they can overheat and cause fires. Consumers should contact the company for a free replacement.
Shilpa Medicare Limited is voluntarily recalling 35,931 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations.
Fresenius Kabi is recalling 13,525 bottles of Dexmedetomidine HCl Injection due to cross-contamination with trace amounts of lidocaine.
Volkswagen is recalling 2012-2014 Beetle and Beetle Convertible vehicles because the driver's side air bag inflator may explode due to propellant degradation.
Shilpa Medicare Limited is recalling 2,008 vials of Docetaxel Injection USP due to Current Good Manufacturing Practice (CGMP) deviations.
Shilpa Medicare Limited is recalling 4,166 bottles of Imatinib Mesylate 400 mg tablets nationwide due to Current Good Manufacturing Practice (CGMP) deviations.
Daimler Trucks North America is recalling 28 electric school buses where the parking brake may release unexpectedly, increasing crash risk.
Shilpa Medicare Limited is recalling 6,560 vials of Azacitidine for Injection due to Current Good Manufacturing Practice (CGMP) deviations. The recall is voluntary and nationwide.
JMH International is recalling Chef Myron's Premium Teriyaki Sauce because it contains wheat-derived gluten despite a gluten-free claim.
Clinical Innovations is recalling ROM Plus Collection Kits because incorrect swabs may cause false test results.
Camp Chef is recalling about 20,600 portable gas stoves because a sharp edge on an internal gas regulator part can cause gas leaks, posing a fire hazard.
Medtronic is recalling 71,030 Evolut PRO System units worldwide due to a potential for transcatheter aortic valve leaflet damage during post-implant balloon dilatation.
Mani, Inc. is recalling Trocar Kit 23G S units because Luer connector dimensions are out of specification, which may cause fluid leakage or disconnection during ophthalmic surgery.
Graco is recalling inclined sleeper accessories for four playard models due to a risk of infant suffocation. Consumers should stop using the accessory immediately and contact Graco for a refund.