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.
RXBAR is voluntarily recalling Kids Chocolate Chip bars because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR 12-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Porsche is recalling one 2019 Cayenne Turbo because shock absorber forks may allow the shock absorbers to loosen, potentially impairing steering.
Chicago Bar Company LLC is voluntarily recalling RXBAR KIDS Apple Cinnamon Raisin bars because they contain undeclared peanut.
Chicago Bar Company LLC is voluntarily recalling RXBAR Apple Cinnamon bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.
Chicago Bar Company LLC is voluntarily recalling KIDS Berry Blast bars because they contain undeclared peanut, a major food allergen.
Promise Pharmacy, LLC is recalling 8 vials of Pyridoxine HCl Injection due to a lack of sterility assurance. The product was distributed nationwide in the USA.
Chicago Bar Company LLC is voluntarily recalling RXBAR 10-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Mint Chocolate bars due to an undeclared peanut allergen. The recall affects single, 4-count, and 12-count cartons.
Crate and Barrel is recalling Holiday Bear Acrylic Milk Bottles because the included plastic straw can crack or break, posing a laceration hazard.
Chicago Bar Company LLC is voluntarily recalling RXBAR Coffee Chocolate bars due to undeclared peanut. Consumers should check Best By dates and stop eating the product.
Chicago Bar Company LLC is voluntarily recalling Coconut Chocolate RXBARs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR 14-Bar Variety Packs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR variety packs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Chocolate Hazelnut bars due to undeclared peanut. Consumers should stop eating these bars.
Porsche is recalling 14,110 vehicles because the instrument cluster may fail to warn drivers when brake pads are worn out, increasing crash risk.
Volkswagen is recalling 2019 Jetta vehicles because an incorrect driver frontal airbag may have been installed during a service visit, potentially increasing injury risk in a crash.
Cincinnati Sub-Zero is recalling 396 Hemotherm CE Dual Reservoir Cooler/Heater units because fuse clips may stretch, causing overheating and device shutdown.
Signature Orthopedics is voluntarily recalling three Genius Knee Cemented CR Femoral Components due to a product mix-up. The devices were distributed in Florida, New York, and Tennessee.
Chicago Bar Company LLC is voluntarily recalling RXBAR Mango Pineapple bars because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling Chocolate Sea Salt RXBARs because they contain undeclared peanut, a major food allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Maple Sea Salt bars due to an undeclared peanut allergen.
Chicago Bar Company LLC is voluntarily recalling RXBAR Blueberry bars due to the presence of undeclared peanut, a major food allergen.
Philips is issuing a software update for 24 Ingenuity TF PET/CT systems to correct multiple issues identified in the previous software version.
Ottobock is recalling 538 PushValve units because some valve inserts have a diameter smaller than the specification. The valve is used for prosthetic fitting of lower limb amputees.