State
73,381 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 73,381 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling 2021-2022 F-150 vehicles because underbody insulators may loosen and damage the driveshaft, potentially causing loss of vehicle control.
Ford is recalling 2022 Transit vehicles with rearview cameras due to a missing audio control module that prevents the camera image from displaying in reverse.
Subaru is recalling 2017-2019 Impreza vehicles because defective reflectors may fail to reflect light adequately, increasing crash risk.
Residential Elevators, Inc. is recalling about 31,000 home elevators sold since 1986 because young children can become trapped between the exterior and interior doors, risking serious injury or death.
Certain 2022 Chrysler Pacifica and Voyager vehicles have improperly tightened windshield wiper arm nuts, causing malfunction. This reduces driver visibility and increases crash risk. Dealers will tighten the nuts free of charge.
Rosenbauer America is recalling 2022 Commander and 2023 Commercial M2-106 fire trucks because an engine control module short-circuit may cause unexpected engine shutdown.
Grand Design is recalling 2023 and 2022 Momentum fifth wheels due to a defective ramp door cut-off switch that may allow the electric ramp door to fall, creating an injury risk.
Future Motion is recalling front footpads for Onewheel GT electric skateboards because the footpad can fail to disengage after the rider dismounts, causing the skateboard to continue operating and potentially injure bystanders.
General Motors is recalling 484,155 vehicles with improperly formed rivets on third-row seat belt buckle assemblies. The defect may prevent proper seat belt restraint in a crash, increasing injury risk.
Kingdom Honey Royal Honey VIP is recalled due to undeclared sildenafil, a pharmaceutical ingredient. The product was distributed nationwide; all lots are affected.
BMW is recalling 2018 540D xDrive vehicles because an internal leak in the EGR cooler may cause coolant to mix with soot, creating smoldering particles and a melting intake manifold that increases fire risk.
Distributor RFR, LLC is recalling SANGTER Energy Supplement Capsules because FDA analysis found they contain undisclosed sildenafil without FDA approval. The product was distributed nationwide and internationally.
Kia is recalling 2016 Sedona and Sorento vehicles because faulty shift lever components may prevent locking, allowing the vehicle to roll away.
North American Diagnostics is recalling SARS-CoV-2 rapid antigen test kits that were distributed without FDA approval or clearance. Approximately 122,366 units were sold to consumers across multiple US states and internationally.
SUSTANGO capsules contain the undisclosed pharmaceutical ingredient tadalafil and were marketed without FDA approval. Approximately 750 cartons were distributed nationwide via Amazon.
The FDA is recalling 399 units of the PRESTIGE RETRACTION GRASPER surgical instrument due to risk of weld separation between the handle and shaft. This defect could cause device malfunction during surgical procedures.
Siemens Atellica CH Iron_2 in vitro diagnostic devices are being recalled because they produce falsely elevated microalbumin test results when a microalbumin test immediately follows an iron test. No illnesses have been reported.
Matzim LA Extended-Release Tablets, 240 mg are being recalled due to failed dissolution specifications. Patients taking this medication should consult their doctor about their treatment.
Procter & Gamble is recalling 90,522 cases of Vicks ZzzQuil Liquid Melatonin Syrup due to being an acidified/low-acid dietary supplement without an FDA-approved manufacturing process.
Aesculap Implant Systems is recalling PRESTIGE ATRAUMATIC GRASPER surgical instruments because the weld connecting the handle to the shaft may separate during use.
Teva Pharmaceuticals is recalling Matzim LA (Diltiazem Hydrochloride) 180 mg tablets because they failed to meet dissolution specifications. The recall affects approximately 8,022 bottles distributed nationwide in the United States and Puerto Rico.
Altec Industries is recalling 2015-2022 DT65 and DT85 Aerial Devices because a weld crack could cause the auger bracket to detach, increasing injury risk.
The Procter & Gamble Company is recalling Vicks Children's Botanicals Liquid Nighttime due to manufacturing without an approved acidification process. The product's preservation safety cannot be assured.
Intuitive Surgical is recalling 505 E-100 electrosurgical generators because required preventative maintenance was not performed on units distributed worldwide and in the US.
St. Jude Medical recalls Merlin 2 PCS model MER3700, software used to program and interrogate Abbott implantable medical devices.