State
73,366 recalls have nationwide distribution and so reach South Dakota. 2,684 additional recalls listed South Dakota specifically in their distribution scope.
Of the 2,684 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 2,684 recalls whose distribution notice names South Dakota specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Subaru is recalling 2009-2013 Forester vehicles because the front seat belt force-limiter may not operate correctly in a crash, increasing injury risk.
Generac and DR 6500- and 8000-watt portable generators are being recalled because an unlocked handle can pinch and amputate fingers. The firm has received 37 injury reports, including 24 finger amputations.
Shyft Group is recalling 2022 Utilimaster Walk-In vans because the catalytic converter cover may damage brake lines, increasing crash risk.
Mockingbird Single-to-Double Strollers may have cracks in the frame that pose a fall risk to children. The manufacturer has received 138 reports of frame cracks, including 8 injuries, and is offering free frame reinforcement kits.
Toyota is recalling specific front seat belt assemblies sold as replacement parts because the force-limiter may not operate correctly, increasing injury risk in a crash.
Navistar is recalling 2023 International MV vehicles because locking clips on the wheel hub retaining nut may be damaged, causing the wheel hub to loosen and separate from the axle housing, which increases crash risk.
RAM is recalling certain 2500 and 3500 vehicles due to transmission fluid leaks that could cause fires. Dealers will replace the affected components at no cost.
Hunter Fan Company is recalling approximately 2,600 light fixtures from five collections because internal wires can become damaged, posing an electric shock hazard. Consumers should stop using the products immediately and contact Hunter for a full refund.
The CritiCool thermoregulation device may experience premature pump failure leading to a HALT 4 error from which the device cannot recover, potentially delaying treatment. One death has been reported.
Holiday Rambler and Fleetwood motorhomes (2022–2023) have interior step treads that may be improperly secured and can detach when stepped on, creating a fall hazard.
Medline Industries is recalling 300 units of Bausch + Lomb Cataract Packs due to breather pouches with seal openings that may compromise sterility. The affected surgical kits were distributed nationwide.
Becton Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together in pouches or fail when used with automated loaders. No illnesses have been reported.
MICROVENTION is recalling WEB Detachment Controllers due to an out-of-specification tunnel opening that may prevent proper implant detachment. This defect could delay treatment and cause vessel damage from implant manipulation.
Medline Industries is recalling 800 Bausch + Lomb Basic Ophthalmic surgical kits (Lot 22DBN365) for defective breather pouch seals. Opened seals in the packaging compromise the sterile conditions required for surgical procedures.
Bella Cucina Artful Food is recalling Walnut Sage Pesto because milk is present in the product but not declared on the label. Consumers allergic to milk should not consume this product.
Becton, Dickinson is recalling BD Trucount Tubes due to partial label detachment that can cause tubes to stick together or create automation errors. The defect stems from an adhesive supplier change and affects 52,570 units.
Volkswagen is recalling 2023 ID.4 vehicles due to improper electric motor sealing assembly that may allow coolant to leak into the high-voltage system, risking loss of vehicle control and unintended airbag deployment.
Bella Cucina Artful Food is recalling Death By Chocolate Cookies because the labels do not declare milk and wheat, which are common allergens. Consumers with allergies to these ingredients are at risk.
SenTec AG voluntarily recalled 17,208 units of transcutaneous CO2/O2 monitor attachment rings due to weak skin adhesion. The devices, used in noninvasive patient monitoring, were distributed nationwide.
Medline is recalling approximately 160 surgical kits with defective breather pouches showing seal openings, potentially compromising sterility. The recall affects facilities in eight states nationwide.
Volkswagen is recalling 2016 Golf R vehicles because incorrect software may prevent windshield wipers from activating, increasing crash risk.
Edwards Lifesciences is recalling 715,620 Fogarty Arterial Embolectomy Catheters due to confirmed latex deterioration in the pouch packaging. The material degradation could affect device performance during use.
Bella Cucina Artful Food Arugula & Pine Nut Pesto jars do not properly disclose milk on the label despite containing the allergen. The FDA Class II recall affects multiple lot numbers distributed nationwide and internationally.
Bella Cucina Artful Food is recalling its Preserved Lemon Cream because the label does not indicate the presence of milk, posing a risk to consumers with milk allergies.
Johnson & Johnson is recalling 91 THERMOCOOL SMARTTOUCH SF cardiac catheters nationwide due to manufacturing defects introducing cellulose fibers into the irrigation system. The contamination may prevent proper flushing, reduce cooling capability, or cause clotting complications.