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.
Jayco is recalling 2018 Eagle HT fifth wheel trailers because a spindle placement error in the pin box may cause the bearing to become loose, increasing the risk of a crash.
Navistar is recalling 2019 IC Bus CE school buses because an improperly routed air supply line may cause unintentional parking brake modulation, increasing crash risk.
Navistar is recalling 2017-2019 International HX trucks because an improperly routed air supply line may cause unintentional parking brake modulation, increasing crash risk.
Daimler Vans USA is recalling 2017 Mercedes-Benz and Freightliner Sprinter 2500 and 3500 vans because missing spot welds may reduce body strength in a crash.
General Motors is recalling 2015-2016 Chevrolet Tahoe and Silverado 1500 Police Pursuit and Special-Service vehicles because the driver's seat belt pretensioner cable may fatigue and break, increasing injury risk in a crash.
Starcraft RV is recalling 508 camping trailers because a power roof lift mechanism may be damaged by misuse, potentially causing the roof to fall.
Jayco is recalling 2011 and 2013 Jay Series camping trailers because misuse of the manual roof lift override may damage the mechanism, causing the roof to fall unexpectedly.
Coastal Meds, LLC. is recalling 1,506 vials of Hydroxocobalamin Injectable due to the presence of unknown particulate matter. The product was distributed nationwide.
Seabear Company is recalling 2,080 units of Cold Smoked Wild Coho Salmon Lox due to water phase salt deviations and mislabeled storage instructions.
Premier Pharmacy Labs is recalling specific lots of Morphine Sulfate Injection because routine testing of other lots detected microbial contamination risks.
Coastal Meds, LLC. is recalling 635 vials of Pyridoxine Injectable due to the presence of unknown particulate matter.
NGB Corp is recalling Nxtgen Botanicals Maeng Da Kratom dietary supplements due to potential Salmonella contamination.
Coastal Meds, LLC. is recalling LIPO-PLEX Injectable-30 mL vials nationwide due to the presence of unknown particulate matter.
Premier Pharmacy Labs Inc is recalling 4,192 syringes of Morphine Sulfate 4 mg/mL PF Injection due to a lack of assurance of sterility.
Becton Dickinson is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.
Thor Motor Coach is recalling 2011-2017 Tuscany and Venetian motorhomes because an incorrectly routed power steering hose may cause electrical arcing and a fire.
Seabear Company is recalling 381 units of Hot Smoked Keta Beergarden Salmon due to water phase salt deviations and mislabeled storage instructions.
Premier Pharmacy Labs is recalling 3,570 hydromorphone syringes because routine testing of other lots found microbial contamination risks.
Volkswagen is recalling 2018 Atlas vehicles because a manufacturing error may cause the fuel tank to leak, increasing the risk of a fire.
Coastal Meds, LLC. is recalling 3,733 vials of LIPO-DEN EXTREME Injectable-30 mL due to the presence of unknown particulate matter.
Coastal Meds, LLC. is recalling 200 vials of ADENO-PLEX Injectable-30 mL MDV due to the presence of unknown particulate matter.
Premier Pharmacy Labs is recalling NeoStigmine Methylsulfate syringes because routine testing of other lots detected microbial contamination risks.
Coastal Meds, LLC. is recalling 1,457 vials of LIPO-DEN PLUS Injectable because of the presence of unknown particulate matter. The product was distributed nationwide in the USA.
Bayer is recalling specific Alka-Seltzer Plus packages because the ingredients listed on the front sticker may not match the actual product inside the carton.
Becton Dickinson & Company is recalling BD Vacutainer Push Button Blood Collection Sets because they do not meet the labeled sterility assurance level.