State
73,478 recalls have nationwide distribution and so reach South Dakota. 2,686 additional recalls listed South Dakota specifically in their distribution scope.
Of the 2,686 recalls naming South Dakota we have scored against our rubric, 401 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 747 (28%) are Severe.
Which agencies issued them
These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,478 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Sun Pharmaceutical Industries is recalling Pregabalin 50 mg capsules due to out-of-specification results in particle size distribution and bulk density of the active pharmaceutical ingredient.
Perrigo Company PLC is recalling Rite Aid Allergy Relief Fexofenadine Hydrochloride 180mg tablets nationwide due to failed impurity specifications. An out-of-specification result for impurity A was found during stability testing.
Perrigo Company PLC is recalling basic+care allergy Fexofenadine Hydrochloride Tablets (180 mg, 150-count bottles) distributed nationwide because impurity testing results exceeded specification limits during stability testing.
Ascend Laboratories recalls Cefixime 400 mg capsules due to failed impurities and degradation specifications. The affected 42,698 bottles were distributed nationwide.
Perrigo Company PLC is recalling basic+care allergy Fexofenadine Hydrochloride Tablets, 60 mg, 100-count bottles, due to out-of-specification impurity levels detected during stability testing.
Amazon Basic+Care Allergy Fexofenadine Hydrochloride Tablets (60 mg, 100-count) are being recalled because impurity levels exceeded acceptable limits during stability testing. The recall affects 38,352 bottles distributed nationwide.
Perrigo Company PLC is recalling TopCare Allergy Relief Fexofenadine Hydrochloride 180mg tablets in multiple pack sizes due to failed impurity specifications during stability testing. The affected lots were distributed nationwide.
Perrigo Company PLC is recalling Health Mart Fexofenadine Hydrochloride 12HR 60mg tablets due to impurity A exceeding specification limits during stability testing. The recall affects 12,384 containers distributed nationwide.
Amazon-branded Allergy Fexofenadine Hydrochloride Tablets 180 mg are being recalled because testing found an out-of-specification impurity during stability testing.
CVS Allergy Relief Fexofenadine Hydrochloride Tablets 60 mg are being recalled because stability testing found an out-of-specification result for impurity A. The recall affects approximately 138,144 containers distributed nationwide.
Oshkosh is recalling 2019-2022 S-Series vehicles because front axle u-bolts may fail, potentially allowing the axle to shift or detach and increasing crash risk.
Bella residential elevators pose a risk of child entrapment between exterior and interior doors. Young children can become trapped and suffer serious injuries or death when the elevator moves to another floor.
Savaria and Garaventa residential elevators pose an entrapment risk to young children due to gaps between doors. Young children can become trapped and suffer serious injury or death when the elevator is called to another floor.
Play-Mor is recalling specific 2017-2020 trailers because a propane regulator may fail, increasing pressure and fire risk. Dealers will replace the parts free of charge.
Inclinator Company of America is recalling residential elevators manufactured from 1979 through 2021 because young children can become entrapped between the exterior landing door and interior elevator car door, risking serious injury or death.
Oshkosh is recalling 2019-2022 S-Series vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.
Reading Truck Body is recalling 2017-2021 Marauder Landscape Dump Body vehicles because a rear pivot mount weld may fail, increasing injury risk.
Abbyland Foods is recalling approximately 14,976 pounds of smoked beef sticks because they contain undeclared milk, a known allergen.
Lakota is recalling 2021-2022 Bighorn, Charger, and Livestock trailers because certain tires may experience belt separation, increasing crash risk.
Forest River is recalling 2021-2022 Aurora and Catalina travel trailers because the panel sealing the cooktop from the furnace was not properly sealed, which could cause an inverted flame and fire risk.
Forest River, Inc. is recalling certain 2021-2022 fifth wheel trailers equipped with defective Sailun tires that may experience belt separation. The defect could cause loss of vehicle control and increase the risk of a crash.
Interstate Meat Dist. Inc. is recalling approximately 28,356 pounds of ground beef products due to possible E. coli O157:H7 contamination.
Polaris is recalling about 1,100 Model Year 2022 Outlaw 110 EFI Youth ATVs because the inner layer of the fuel line can leak, posing a fire hazard. No fires or injuries have been reported.
Kettle River Products is recalling approximately 1,464 pounds of chicken alfredo pizza due to misbranding and an undeclared wheat allergen. No adverse reactions have been reported.
Colony Brands is recalling about 20 covered wood wagons sold through Montgomery Ward's and Ginny's from September to October 2021 because paint on the wood, plastic handles, and red plastic cover contains excessive lead that can be toxic if ingested by young children.