State
73,741 recalls have nationwide distribution and so reach Rhode Island. 3,053 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,053 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 3,053 recalls whose distribution notice names Rhode Island specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Valeant Pharmaceuticals is recalling 306 cartons of Diazepam Rectal Gel because the outer cartons are missing lot numbers and expiration dates.
Right Value Drug Stores is recalling 4,800 Testosterone 200 mg Pellets because the label contains an incorrect expiration date.
Akoury is recalling AK88S motorcycle helmets because they may not adequately protect the wearer in a crash, increasing the risk of injury.
Koehler-Bright Star is recalling about 7,500 WorkSafe 3-D cell flashlights because a missing circuit board component poses an explosion hazard.
Erwin Hymer is recalling 2015-2018 Roadtrek Zion motorhomes because sofa installation may have damaged the rear brake line, increasing stopping distance and crash risk.
Erwin Hymer is recalling 2017-2018 Roadtrek motorhomes because the diesel fuel tank may have been damaged during seat installation, increasing fire risk.
Forest River is recalling specific 2018-2019 recreational trailers because the awning may deploy while moving, increasing the risk of a crash.
Cummins is recalling ISX15 and X15 diesel engines because a restricted fuel pump screen can cause the nylon fuel line to burst, leading to fuel leaks or engine stalling.
KZRV is recalling 2018-2019 Sportsmen 333BHK travel trailers because liquid propane lines routed through the wheel well may be damaged by road debris, increasing fire risk.
TRW is recalling specific outer tie rods sold as replacement parts for 1988-2000 GM vehicles because the locking nut may fail, causing a loss of steering.
Daimler Trucks North America is recalling 2018-2019 Freightliner trucks because brake caliper mounting bolts may be loose, which can reduce braking effectiveness and increase crash risk.
Chrysler is recalling specific 2018-2019 Dodge and Jeep vehicles because rear brake caliper pistons may have insufficient coating, potentially reducing braking performance.
FCA US LLC is recalling specific 2017-2019 Chrysler, Jeep, Ram, Dodge, and Fiat vehicles because a faulty voltage regulator chip may cause the vehicle to stall or fail to start.
Harbor Freight Tools is recalling about 25,000 electronic handgun safes because they can open upon impact, posing a serious injury risk to children.
Vitamix is recalling Ascent and Venturist series blending containers because they can separate from the blade base, exposing blades and posing a laceration hazard.
Gillig is recalling 2012-2018 Low Floor buses because front and rear turn signals may flash at different rates, potentially confusing other drivers.
LL'S Magnetic Clay Inc. is recalling Prescript-Assist Probiotic & Prebiotic supplements because they may contain undeclared almonds, shellfish, milk, eggs, or peanuts.
Daimler Trucks North America is recalling 2018-2019 Freightliner Cascadia trucks because pitman arms may crack and fracture, potentially causing a loss of steering control.
GE Healthcare is recalling 42 Optima CT 520 units because they may not be properly wired to the uninterruptible power supply.
GE Healthcare is recalling 42 Optima CT 540 units because they may not be properly wired to the uninterruptible power supply.
Pfizer is recalling Daptomycin for Injection due to reports of adverse events indicative of infusion reactions related to microbiological contamination.
Integra LifeSciences is recalling Mayfield Infinity XR2 Low Profile Base Units because the knob assembly in the swivel adapter may fracture or break during use.
Griffith Labs U.S.A. is recalling 50-pound bags of Herb Crouton Seasoning due to the potential presence of Salmonella from a recalled whey ingredient.
Zimmer Surgical Inc is recalling 140 units of the Zimmer Dermatone AN skin graft device due to a loose control bar that may compromise graft thickness control.
Griffith Labs U.S.A. is recalling Low Sodium Brown Gravy Mix due to the potential presence of Salmonella from a recalled whey ingredient.