State
73,363 recalls have nationwide distribution and so reach Arkansas. 5,542 additional recalls listed Arkansas specifically in their distribution scope.
Of the 5,542 recalls naming Arkansas we have scored against our rubric, 1,029 (19%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,222 (22%) are Severe.
Which agencies issued them
These figures cover only the 5,542 recalls whose distribution notice names Arkansas specifically. The 73,363 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Noven Pharmaceuticals recalls Daytrana (methylphenidate) 30 mg transdermal patches nationwide due to defective delivery system components that fail shear specifications. Patients should contact their healthcare provider regarding medication alternatives.
Noven Pharmaceuticals is recalling specific lots of Daytrana (methylphenidate) transdermal patches due to a defective delivery system that is out of specification for shear. Affected lots are Lot 91956 (6/2023) and Lot 92475 (7/2023), distributed nationwide.
DePuy Orthopaedics is recalling 7 units of the Attune Revision Tibial Insert that received excess gamma radiation during manufacturing, which may degrade implant material properties.
Boehringer Ingelheim Pharmaceuticals is recalling Jardiance (Empagliflozin) 25 mg tablets due to a label mix-up affecting 69,375 bottles distributed nationwide.
CareFusion recalls 7,914 units of BD Pyxis automated medication dispensing systems after firmware was inadvertently downgraded during installation, potentially causing drawer failures and medication delivery delays.
BA Sports Nutrition is recalling BODYARMOR SportWater due to potential plastic pieces in the product. The recall affects approximately 21 million bottles distributed across 11 states.
Volkswagen is recalling certain 2022 Taos vehicles because the fuel delivery pump may break and cause a sudden engine stall, increasing the risk of a crash.
DePuy Orthopaedics recalls 7 units of Attune Revision LPS Tibial Inserts (Part 151760118, Lot JP6452) distributed worldwide due to excessive gamma radiation during manufacturing. This overage may result in material property changes.
DePuy Orthopaedics is recalling 7 units of the Attune Revision Limb Preservation System Tibial Insert (Lot JP9022) that received higher than specified gamma radiation doses. The over-irradiation may cause changes to implant material properties.
DePuy Orthopaedics is recalling Attune Revision LPS Tibial Insert devices (Lot JP9016) because they received excessive gamma radiation during manufacturing, which may compromise material properties.
Noven Pharmaceuticals is recalling Daytrana methylphenidate transdermal patches for a defective delivery system that fails to meet shear specifications. The recall affects specific lots distributed nationwide.
Withings Scan Monitor/ScanWatch (model hwa09) has a software defect preventing physicians from reviewing ECG recordings, which is critical to the device's FDA clearance requirement for physician-supervised use. Users should discontinue use until the defect is corrected.
DePuy Orthopaedics is recalling Attune Posterior tibial insert implants that received excessive gamma radiation during manufacturing, which may degrade the material properties of the knee replacement component.
DeRoyal SafeLiner Suction Canister model PHESL-1000B is being recalled due to lid shrinkage that prevents proper vacuum seal formation and maintenance. The recall affects 27,200 devices distributed across multiple US states.
CooperVision is recalling Clariti 1-day toric contact lenses from lot W0124677 because they were made with a misaligned axis that results in incorrect lens power.
Sun Pharmaceutical is recalling 1,920 bottles of Dofetilide Capsules (500 mcg) nationwide due to failed content uniformity specifications, meaning the capsules do not contain uniform amounts of active ingredient.
Noven Pharmaceuticals is recalling specific lots of Daytrana methylphenidate transdermal patches distributed nationwide because the delivery system is out of specification for shear. The affected lots require patient and healthcare provider attention.
Daimler Trucks North America is recalling 2020-2021 Freightliner Cascadia and Western Star 49X vehicles because hazard warning lights may flash improperly during Advanced Braking Assist events, potentially confusing other drivers and increasing crash risk.
Hyundai is recalling 575 units of the 2023 Genesis G90 because the seat belt pretensioners may explode in a crash. Metal fragments from the explosion may strike and injure vehicle occupants.
Cummins is recalling PowerDrive 7000 electric drive systems because the control module may cause vehicles to reverse faster than expected, increasing crash risk.
Vermeer is recalling 2021-2023 BC700XL brush chipper trailers because an incorrect retention bolt in the safety chain assembly may allow the chain to detach, increasing crash risk.
Shadow Trailer is recalling 2016-2023 Living Quarter trailers because cooktop burner tubes may fracture and leak gas, increasing fire risk.
Forest River is recalling 2023 Pause travel trailers because an incorrectly routed brake wire may pinch, potentially causing brake failure and increasing crash risk.
Forest River is recalling 2023 Pause travel trailers because a wiring error may prevent the breakaway switch from activating trailer brakes, increasing crash risk.
Ford is recalling certain 2023 Edge vehicles because child seat tether welds may be insufficient, potentially reducing proper child restraint during a crash. Dealers will replace the seat back frame free of charge.