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.
Honda is recalling specific 2006-2015 models because the passenger frontal air bag inflator may explode due to propellant degradation, posing a risk of serious injury or death.
Dolan Northwest is recalling Design Classics chandeliers because the top loop can break, causing the fixture to fall and pose impact and laceration risks.
Mazda is recalling 262,220 vehicles due to a software error that may cause the engine to stall unexpectedly, increasing crash risk.
Gillette is recalling Venus Simply3 disposable razors because manufacturing errors caused blade misalignment, posing a risk of cuts during normal use.
Fisher-Price is recalling inclined sleeper accessories for Ultra-Lite Day & Night Play Yards due to safety concerns about infant sleep on inclined surfaces.
BRP is recalling Sea-Doo marine coolers because the latch can lock automatically, posing entrapment and suffocation risks. No injuries have been reported.
Teleflex Medical is voluntarily recalling specific lots of Sheridan LTS tracheal tubes because the 15 mm connector may disconnect from the tube.
Cook Inc. is recalling 131 Advance Enforcer 35 Focal Force PTA Balloon Catheters because multiple complaints reported the balloons bursting below their rated pressure.
Monarch Medical Technologies is recalling EndoTool IV software versions 1.8 through 1.10 because insulin dosing calculations were erroneously high.
GE Healthcare is recalling 1,113 Discovery ML DR PET/CT systems because the table may stop moving without stopping X-ray exposure.
GE Healthcare is recalling 1,113 Discovery ML PET/CT systems because the table may stop moving without stopping X-ray exposure.
Teleflex Medical is voluntarily recalling specific lots of Sheridan Novaplus endotracheal tubes because the 15 mm Sheridan connector may disconnect from the tube.
APS BioGroup is recalling Immuno PRP Spray because testing found elevated levels of Stenotrophomonas maltophilia. The product was distributed nationwide and in Switzerland.
APS BioGroup is recalling DPS Throat Spray because testing found elevated levels of Stenotrophomonas maltophilia bacteria.
FDA is recalling 3,113,280 units of the EGIA 60 Articulating Medical Stapler due to missing pin components that may cause incomplete staple formation and serious surgical complications.
P & L Developments, LLC is recalling 17,664 bottles of Cetirizine Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, potentially leading to serious surgical complications.
Teleflex Medical is voluntarily recalling specific lots of Hudson RCI Sheridan tracheal tubes because the 15 mm connector may disconnect from the tube.
Zydus Pharmaceuticals USA Inc. is recalling Pramipexole Dihydrochloride Tablets 0.125 mg due to cross-contamination caused by cleaning failures.
Whole Foods Market is recalling sun-dried tomato pesto because the labels failed to declare milk, walnuts, and pine nuts.
P & L Developments is recalling 124,512 bottles of Up & Up Children's Cetirizine Oral Solution due to potential contamination with Burkholderia cepacia and Ralstonia pickettii.
Zydus Pharmaceuticals is recalling Anastrozole tablets due to cross-contamination from cleaning failures. The recall covers 1.4 million bottles distributed nationwide.
Covidien LLC is recalling Signia Tri-Staple 2.0 reloads because missing pin components may cause incomplete staple formation, leading to serious surgical complications.
The FDA is recalling 3,113,280 units of the EGIA 60 Articulating Extra Thick Sulu device due to a missing pin component that may cause incomplete staple formation and serious surgical complications.
Nissan is recalling 2017-2019 Titan vehicles because a damaged alternator harness may cause an electrical short, increasing the risk of engine stall or fire.