State
73,198 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 567 (21%) are Severe.
Which agencies issued them
These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,198 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Ford is recalling certain 2018-2023 Lincoln Navigator and Aviator vehicles, 2022-2023 Ford Transit, and 2021 Ford Bronco vehicles. The rearview camera may fail to display when reversing, reducing visibility and increasing crash risk.
Ford is recalling certain 2023 Edge vehicles. The front right headlight may be too bright or aimed incorrectly, which may cause glare and increase crash risk.
Audi is recalling certain 2019-2021 A6 and A7 models, plus 2021 A6 Allroad and S-series models, for an incorrectly labeled brake fluid cap that could result in reduced braking ability.
The Occupant Detection System (ODS) in certain 2024 Hyundai Palisade vehicles may fail to detect occupants and deactivate the passenger-side front air bags. This increases the risk of injury during a crash in affected vehicles.
Ford is recalling certain 2023 Explorer vehicles with 2.3L GTDI engines because the turbocharger oil supply line may be damaged, causing oil leaks that increase the risk of engine fire or stall.
Streamline Industries is recalling LA Chopper Brake Hose Kits because the hydraulic hoses may fail, potentially causing a loss of braking ability and increasing crash risk.
Harley-Davidson is recalling specific rear shock absorbers because a fastener may break, allowing the adjuster to damage the tire and cause a loss of pressure.
Kia is recalling specific 2016-2018 Optima and Rio vehicles because a cracked trunk latch base may prevent the trunk from opening from the inside, potentially trapping occupants.
About 22,000 Aiper Elite Pro GS100 robotic pool vacuum cleaners are being recalled because the battery can overheat and catch fire when the charging cord is plugged in without the adapter. The manufacturer is replacing all recalled units with a different model.
Ecnup kids bike helmets sold on Amazon do not meet federal safety standards for coverage, stability, and labeling. The helmets can fail to protect the head in a crash.
Covidien is recalling MAHURKAR dialysis catheters because the center lumen may be blocked by excess silicone lubricant. This could delay treatment and cause blood clots, hemolysis, or embolism.
Alcon is recalling 444,372 units of Phaco Standalone Tips worldwide because the plastic wrench included with the product can generate plastic debris when over-tightened, potentially injuring patients.
Covidien LP is recalling MAHURKAR dialysis catheters due to excess silicone lubricant that can block the central lumen, potentially delaying treatment or causing serious complications.
Covidien is recalling MAHURKAR Triple Lumen Acute Dialysis Catheters due to excessive lubricant blocking the center lumen, which may delay dialysis and cause blood clots. The recall affects 6,949 units distributed in the US and worldwide.
Covidien recalls 519 MAHURKAR acute dialysis catheters (Lot 2200400292) due to excessive silicone lubricant coating the catheter tip that may cause partial or full occlusion and treatment delays.
Covidien is recalling MAHURKAR acute dialysis catheters because the center lumen tip may be occluded by excessive silicone-based lubricant. Obstruction could delay treatment or cause embolism and thrombosis.
Alcon is recalling the Constellation Procedure Pak due to reports of patient injury from plastic debris. The debris can result from over-tightening the device with the included plastic wrench.
Covidien is recalling 1,099 MAHURKAR dialysis catheters worldwide due to excessive silicone lubricant that can block the center lumen, potentially delaying treatment.
The MAHURKAR dialysis catheter is recalled because excessive silicone lubricant can obstruct the center lumen, potentially delaying critical dialysis treatment.
Covidien's Mahurkar dialysis catheters are recalled due to center lumen occlusion from excessive silicone lubricant, risking treatment delay and serious vascular complications.
Covidien is recalling MAHURKAR dialysis catheters that may have excessive lubricant coating the catheter tip, potentially causing dangerous blockages that delay treatment or lead to serious complications.
Yokohama is recalling 6,992 specific 504C tires because a defective splice may allow air to leak into the sidewall, potentially causing a crash.
Covidien is recalling 1,875 MAHURKAR dialysis catheters with lot numbers 2204000239 and 2227800110 due to excessive silicone lubricant causing catheter obstruction. The obstruction may delay treatment or cause hemolysis and thrombosis.
Covidien is recalling dialysis catheters with excessive lubricant in the center lumen, which may cause occlusion, obstruct blood flow, and delay treatment.
Alcon Custom Pak intraocular lens packages are recalled due to reports of patient injury during surgical procedures caused by plastic debris from over-tightening with the included plastic wrench.