State
73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Vygon U.S.A. is recalling 339,800 DUALSTOP Red Caps used for intravascular lines because a defect causes leaks.
Spencer Manufacturing is recalling certain 2017-2019 fire trucks because Whelen accessory brake lights may illuminate without the brake pedal being pressed.
Elekta Limited is recalling 12 Unity MRI-guided radiation therapy systems because acquired images may not represent average anatomy during respiratory motion, potentially affecting treatment accuracy.
Go Couture is recalling about 120 children's loungewear sets because they fail to meet federal flammability standards for children's sleepwear, posing a risk of burn injuries.
Integra Limited is recalling 232 units of bioBLOCK Resorbable Subtalar Implants because temperature indicators suggest exposure to temperatures greater than 110°F.
Roche Diagnostics is recalling 656 COBAS INTEGRA 400 plus analyzers because specific tests require additional wash cycles to prevent carry-over.
Roche Diagnostics is recalling 137 cobas c 111 and COBAS INTEGRA 400 plus analyzers because specific tests require additional wash cycles to prevent carry-over.
Beaver Visitec is recalling 196 boxes of Xstar Slit Knives because the package label indicates a 2.4 mm size, while the device marking shows 2.75 mm.
Conformis, Inc. is recalling two iTotal CR Total Knee Replacement Systems prepared with incorrect patient ID labels and potentially incorrect components.
Integra Limited is recalling 232 units of the bioBLOCK Resorbable Subtalar Implant because temperature indicators suggest exposure to temperatures above 110°F.
Lupin Somerset is recalling Gavilyte-N because orange and cherry flavor packets incorrectly list 'natural lemon flavor' as an ingredient.
Integra Limited is recalling 232 units of the bioBLOCK Resorbable Subtalar Implant because temperature indicators suggest exposure to temperatures above 110°F.
Merical, LLC is recalling Walgreens Probiotic 12.5 Billion Active Cultures because the product contains a different bacterial strain than listed on the label.
X-Gen Pharmaceuticals is recalling Clonidine HCL Injection vials because the side carton incorrectly lists the concentration as 500 mcg instead of 100 mcg per mL.
Auro Pharmacies Inc. is recalling 167 vials of Biotin 10 mg/mL Injection because the product failed to meet its pH label claim.
Medi-Physics Inc. dba GE Healthcare is recalling Thallous Chloride TI 201 Injection vials because trace amounts of an impurity were detected in the manufacturing reagent.
REV is recalling 2019 Fleetwood Flair and Holiday Rambler Admiral motorhomes because the generator exhaust pipe placement may allow carbon monoxide to enter the vehicle.
Fontaine Trailer Company is recalling 2017-2019 Traverse HT trailers because a hydraulic cylinder retaining pin may disconnect, posing a crash risk.
Altec is recalling 2017-2018 aerial devices because turntable fasteners may fail, potentially causing the pedestal and turntable to separate.
H&M is recalling specific children's hooded bathrobes because they fail to meet federal flammability standards, posing a risk of burn injuries.
Triumph is recalling 2016-2018 Thruxton motorcycles because accessory fairing kits may damage wiring, causing loss of lights or engine stalls.
Fisher-Price is recalling all Rock 'n Play Sleepers because over 30 infant fatalities have occurred. Consumers should stop using the product immediately and contact the company for a refund.
Honda is recalling specific 2018-2019 Acura and Honda vehicles because timing belt teeth may separate, potentially causing an engine stall and increasing crash risk.
Honda is recalling 2018-2019 Odyssey vehicles because loose battery connections may cause the transmission to shift to Park, potentially damaging the parking rod and increasing crash risk.
Forest River is recalling 2019 Dynamax Isata motorhomes because brake hoses may lack anti-corrosion plating, risking fluid leaks and loss of braking.