State
73,584 recalls have nationwide distribution and so reach Arkansas. 5,543 additional recalls listed Arkansas specifically in their distribution scope.
Of the 5,543 recalls naming Arkansas we have scored against our rubric, 1,027 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,448 (26%) are Severe.
Which agencies issued them
These figures cover only the 5,543 recalls whose distribution notice names Arkansas specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Subaru is recalling 2021 Outback and Impreza models due to an improperly tightened CVT select lever cable nut that may loosen, causing the gear selector to malfunction and increasing crash risk.
Nissan is recalling 2020 INFINITI QX50 vehicles because the tire and loading information placard may be illegible, potentially leading to incorrect tire installation or overloading.
Brembo is recalling specific brake pads that may corrode and detach, potentially increasing stopping distance and crash risk.
Keystone RV Company is recalling 2021 Dutchmen Voltage trailers because the Federal Identification Tag incorrectly lists tire pressure as 95 PSI instead of 110 PSI, which could cause underinflated tires and increase crash risk.
Keystone RV Company is recalling 2020–2021 Dutchmen Voltage recreational trailers because the Federal Identification Tag lists incorrect tire pressure (110 PSI instead of 95 PSI), which could cause tire overinflation and increase crash risk.
Fresenius Medical Care is recalling 176 drums of Citrasate Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.
Keystone is recalling 2019-2020 Impact recreational trailers because a propane gas leak in the stove can increase the risk of fire.
Boston Scientific is recalling 302 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Boston Scientific is recalling 386 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Sunstar Americas is recalling Paroex Oral Rinse due to potential Burkholderia cepacia complex contamination and manufacturing facility violations.
Edge Pharma, LLC is recalling 71 syringes of Methotrexate USP Sterile Solution for Injection because the media used for post-compounding sterility testing was expired.
Boston Scientific is recalling 319 Lotus Edge Valve Systems because a visual inspection failure may prevent the delivery system from releasing during deployment.
Nostrum Laboratories is recalling Metformin Hydrochloride Extended-Release Tablets, 750 mg, because the product contains N-Nitrosodimethylamine (NDMA) above acceptable intake levels.
Philips is recalling 2,714 Emission Computed Tomography Systems due to a software defect that may cause image misdiagnosis and incorrect patient treatment.
Custom Truck And Body Works is recalling 2020 RAM 4500 and 5500 vehicles because a rear brake line may wear, causing brake failure.
Fresenius Medical Care is recalling Naturalyte Liquid Acid concentrate bottles due to conductivity deviations and calcium concentration below manufacturing specifications.
Siemens is recalling Artis zee, Artis Q, and Artis Pheno systems because the Air Kerma Rate can exceed regulatory limits when frame rates are increased during continuous release.
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Daimler Trucks North America is recalling 2021 Thomas Built Buses Saf-T-Liner HDX and EFX school buses because a brake caliper bolt may be incorrectly tightened, potentially reducing brake effectiveness.
Fresenius Medical Care is recalling NaturaLyte Liquid Acid concentrate bottles because sodium and/or calcium levels were below manufacturing specifications.
Fresenius Medical Care is recalling Naturalyte Liquid Acid concentrate bottles due to conductivity deviations and calcium concentration below specification.
Boston Scientific is recalling 207 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Boston Scientific is recalling 219 Lotus Edge Valve Systems because a visual inspection error could prevent the delivery system from releasing during deployment.
Boston Scientific recalls 278 Lotus Edge Valve Systems due to a failure in visual inspection that prevents proper valve locking during deployment, potentially preventing delivery system release.
Fresenius Medical Care is recalling 198 drums of Citrasate Liquid Acid concentrate because sodium and/or calcium levels were below manufacturing specifications.