State
73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Jayco is recalling 2017 Eagle fifth-wheel recreational vehicles with the dry camping option because the LP manifold can crack, causing a propane gas leak and increasing fire risk.
General Motors is recalling 2006-2010 Pontiac Solstice and 2007-2010 Saturn Sky vehicles because a bent passenger air bag sensor may prevent the air bag from deploying in a crash.
Forest River is recalling 2017 XLR fifth-wheel recreational vehicles because the Federal Placard incorrectly identifies them as Travel Trailers, which may lead to improper towing and increased crash risk.
Triumph is recalling S 4 Alarm Kits and Immobilizers because a leaking battery may cause the engine to stall, increasing crash risk.
Poppie International is recalling Poppies Belgian Eclairs because the milk ingredient may contain Salmonella. The product was distributed in 22 states.
Poppie International is recalling Delizza Patisserie Belgian Custard Cream Mini Eclairs because the milk product used may contain Salmonella.
Porsche is recalling specific replacement gasoline engines because screws may shear off, causing a fuel leak that increases the risk of fire.
Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to complaints of sheath separation, kinking, and tip damage during use.
BioMerieux SA is recalling NucliSENS magnetic extraction reagents because a performance drift was observed in BK virus testing for certain silica batches.
Porsche is recalling 2017 911 and 718 models because fuel collection pipe screws may shear, causing a fuel leak that increases fire risk.
Poppie International is recalling Delizza Patisserie Belgian Mini Chocolate Dipped Cream Puffs because the milk product used may contain Salmonella.
Country Home Products is recalling about 830 DR brand field and brush mowers because a fuel tank valve malfunction can cause gasoline release, posing fire and burn risks.
Advance Engineered is recalling 2014-2015 Dry Bulk Cargo Tank trailers because improperly machined spring brake valves may delay braking, increasing the risk of the trailer rolling away.
Fresenius Medical Care is recalling 2008T Series Hemodialysis Systems because a software error may cause the machine to execute a cancelled ultrafiltration rate instead of the displayed rate.
CareFusion is recalling Alaris Pump Modules and AIL sensor kits because false Air-in-Line alarms can interrupt medication infusions.
Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to reports of sheath separation, kinking, and tip damage during use.
Bard Peripheral Vascular is recalling Halo One 5F Introducer Sheaths due to complaints of separation, kinking, and tip damage during use.
Fresenius Medical Care is recalling 2008K Series Hemodialysis Systems because a software error may cause the machine to execute a cancelled Ultrafiltration Rate setting.
BioMerieux SA is recalling 3,723 units of MagSIL (NucliSENS easyMAG Magnetic Silica) worldwide due to observed performance drift in BK virus testing.
Fresenius Medical Care is recalling 2008K@home hemodialysis systems because a software error may cause the machine to execute a cancelled ultrafiltration rate.
The Binding Site Group is recalling 129 Optilite Analyser units because the lid may fall suddenly and cause injury if not fully open.
Herr Foods is recalling Smoked Chipotle Flavored Kettle Cooked Potato Chips because the seasoning contains a milk ingredient with a potential risk of Salmonella contamination.
The Binding Site Group is recalling Freelite Human Lambda Free Kits due to a calibration curve change that causes an increase in false prozone flags.
Merge Healthcare is recalling Merge Cardio software versions 9.0 through 10.1.2 because a specific user action may cause images to be missing, potentially leading to incorrect diagnosis or treatment.
Great Basin Scientific is recalling the Staph ID/R Blood Culture Panel because the S. aureus probe could result in false positive results.