State
73,809 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 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Motor Coach Industries is recalling 2014-2017 J4500 motor coaches because over-tightened front brake hose clamps may damage the hoses, potentially increasing stopping distance and crash risk.
McNeilus is recalling 2016-2017 Bridgemaster V concrete mixers because the backup alarm and camera may shut off during extended reversing, increasing injury risk.
Mazda is recalling 2004 RX-8 vehicles because a crack in the front suspension lower control arm ball joint socket may cause the ball joint to separate, potentially leading to loss of steering control.
Polaris is recalling 2015-2017 Slingshot vehicles because missing grommets on replacement swingarms may allow debris to contaminate the rear wheel speed sensor, disabling ABS and traction control.
Mazda is recalling 2004-2008 RX-8 vehicles because heat may crack the fuel pump pipe, causing a fuel leak and increasing fire risk.
Kreative Kids is recalling about 7,600 children's robes because they fail to meet federal flammability standards for sleepwear, posing a risk of burn injuries.
Toyota is recalling 2016-2017 Tacoma vehicles with six-cylinder engines because a faulty crank position sensor may cause the engine to stall, increasing crash risk.
Standard Homeopathic Company is recalling Hyland's Baby Nighttime Teething Tablets because FDA analysis found inconsistent amounts of belladonna alkaloids.
Huson Valley Farms is recalling 5,022 jars of Nutty INFUSIONS Roasted Cashew Butter due to Listeria monocytogenes contamination. The product was distributed nationwide through a wholesale in Illinois.
Standard Homeopathic Company is recalling Hyland's Baby Teething Tablets because FDA analysis found inconsistent amounts of belladonna alkaloids that may differ from label claims.
Envy Me is recalling LaBri's Body Health Atomic capsules because the product contains undeclared Sibutramine and was marketed without an approved NDA/ANDA.
Huson Valley Farms is recalling Nutty INFUSIONS Ginger Wasabi Cashew Butter due to Listeria monocytogenes contamination. The product was distributed nationwide through a wholesale in Illinois.
Hospira is recalling 71,550 syringes of Infant 25% Dextrose Injection because human hair was found in an internal sample. The product was distributed nationwide and in Puerto Rico.
EBI Patient Care, Inc. is recalling 33 SpF-PLUS Implantable Stimulators due to higher than allowed cytotoxicity levels found during routine process monitoring.
Spartan Motors is recalling 2010-2014 K2, K3, and Gladiator chassis because a starter motor component may break, causing overheating and increasing fire risk.
Lords Organics is recalling Organic Veda brand Ginger Powder because it may be contaminated with Salmonella. The recall covers 96 units distributed nationwide.
Pierce Manufacturing is recalling 2012-2017 fire trucks because a rear sway bar may detach, increasing crash risk during steering.
EBI Patient Care is recalling 33 SpF-XL IIB implantable stimulators because routine monitoring found higher than allowed cytotoxicity levels.
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing the risk of infection.
Cardinal Health is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Cardinal Health is recalling Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially compromising sterility and increasing the risk of infection.
Cardinal Health 200, LLC is recalling Jackson-Pratt Hemaduct Silicone Round Drains because the product seal may be compromised, potentially compromising sterility and increasing infection risk.
Cardinal Health is recalling specific lots of Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially increasing the risk of infection.
Cardinal Health 200, LLC is recalling specific lots of Jackson-Pratt Silicone Flat Drains because the product seal may be compromised, potentially increasing the risk of infection.
GlaxoSmithKline is recalling specific lots of Ventolin HFA inhalers because some units have out-of-specification leak rates.