State
72,940 recalls have nationwide distribution and so reach Rhode Island. 3,043 additional recalls listed Rhode Island specifically in their distribution scope.
Of the 3,043 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 570 (19%) are Severe.
Which agencies issued them
These figures cover only the 3,043 recalls whose distribution notice names Rhode Island specifically. The 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Alembic Pharmaceuticals is recalling 4,884 bottles of Fesoterodine Fumarate Extended-release Tablets 4 mg because Diester Impurity levels exceeded the specification limit.
DermaRite Industries is recalling 576 containers of Hand-E-Foam because it was made at the same facility where other products and lots were found to be contaminated.
DermaRite Industries is recalling 3,178 bottles of 4-N-1 Skin Protectant No Rinse Wash Cream because it was made at the same facility where other products were found contaminated.
DermaRite Industries is recalling 15,267 cartridges of KleenFoam Antimicrobial Foam Soap because it was made at the same facility where other products were found contaminated.
ASP Global is recalling 6,600 SAFE-T-FILL micro capillary blood collection tubes, 300 microlitres with clot activator, over an inadequate quality system.
ASP Global is recalling 947,100 SAFE-T-FILL plastic blood gas capillary tubes, 150 microlitres with sodium heparin, over an inadequate quality system.
ASP Global is recalling 1,000 SAFE-T-FILL plastic blood gas capillary tubes, 115 microlitres with sodium heparin, over an inadequate quality system.
ASP Global is recalling 50,050 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with clot activator and serum separator gel, over an inadequate quality system.
ASP Global is recalling 209,000 SAFE-T-FILL microhematocrit capillary tubes, 50 microlitres untreated, over an inadequate quality system with unvalidated processes.
ASP Global is recalling 397,000 SAFE-T-FILL plastic blood gas capillary tubes, 150 microlitres, because they were manufactured under an inadequate quality system with unvalidated processes.
ASP Global is recalling 2,100 SAFE-T-FILL micro capillary blood collection tubes, 200 microlitres with sodium fluoride, over an inadequate quality system.
DermaRite Industries is recalling 37,272 tubes of Renew PeriProtect because it was made at the same facility where other products and lots were found to be contaminated.
DermaRite Industries is recalling 2,389 bottles of DermaSarra external analgesic because it was made at the same facility where other products and lots were found to be contaminated.
Polymedco is recalling 403 units of OC-Auto FOBT-CHEK Negative Controls because the kit box and vial labels state an expiration date of 2026-01-16 instead of 2027-01-17.
Rivian is recalling certain 2022-2025 EDV vehicles because the driver's seat belt pretensioner cable may become damaged and fail to restrain the occupant as intended in a crash.
International is recalling certain 2016-2026 trucks with Bendix control units because electrical noise may cause the ECU to misprocess commands or stop working, disabling ABS and stability control.
Volvo is recalling 2018, 2025, and 2026 XC60 vehicles because front seat bolts may be loose. This defect could prevent seats from restraining occupants during a crash.
General Motors is recalling certain 2026 Cadillac Vistiq electric vehicles because the radio may not have been configured to download the electronic owner's manual during production. Without access to the manual, owners may not know how to safely use and operate the vehicle.
General Motors is recalling certain 2026 Chevrolet Silverado 1500, 2500, and 3500 vehicles because some may not have received an owner's manual during production. Without the manual, owners may not know how to safely use child restraint anchorages, increasing crash injury risk.
Bentley is recalling 2023 Bentayga Hybrid vehicles because the high-voltage battery may overheat while charging, increasing the risk of a fire.
Foretravel is recalling 2020-2022 Realm and 2022 Realm 450 vehicles because a seat mounting plate may be improperly welded, allowing the seat to detach.
Newell Coach Corp. is recalling 2022 P50 coaches because improperly welded pedestal mounting plates may cause seat assemblies to detach, increasing crash injury risk.
Pleasant Valley is recalling 2025-2026 nuCamp trailers because incorrect weight information on labels may lead to unintentional overloading and increased crash risk.
PT. Multistrada Arah Sarana, Tbk is recalling Achilles ATR Sport 2 tires because the Tire Identification Number is too long to register, failing federal safety standards.
Altec is recalling 2019-2024 AT Series vehicles because the lower emergency stop may not function when the upper control is selected, increasing the risk of death or serious injury.