State
72,919 recalls have nationwide distribution and so reach South Dakota. 2,681 additional recalls listed South Dakota specifically in their distribution scope.
Of the 2,681 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 565 (21%) are Severe.
Which agencies issued them
These figures cover only the 2,681 recalls whose distribution notice names South Dakota specifically. The 72,919 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Lucid is recalling 2025-2026 Gravity vehicles because second-row seat belt anchor brackets may have insufficient welds, increasing injury risk in a crash.
CCCEI power strips are being recalled because they do not contain supplementary overcurrent protection, creating a fire risk if overloaded. Two reports of sparking and melting have been received.
ABC Bus is recalling specific Van Hool bus models because the front entrance door window may have incorrect glazing, which could reduce driver visibility and increase crash risk.
MPINOI adult portable bed rails are being recalled because users can become entrapped within the rail or between the rail and mattress, and the rails lack the required hazard warning labels.
DuraTrac is recalling stainless steel gas connectors sold between May and November 2025 because a manufacturing defect could cause a gas leak, posing a fire hazard.
Chrysler is recalling certain 2022–2026 Voyager and Pacifica vehicles because the right and left side curtain airbags may have insufficient pressure retention due to improperly sealed seams, increasing the risk of ejection and injury during a crash.
Plunge Buddy is recalling DIY Sauna Heater Kits because electrical conductors within the kits can overheat. Twelve reports of overheating have been received, with no fires or injuries.
Sunnyyes LED mini lights are being recalled because the lithium coin batteries can be easily accessed by children, the remote battery compartment screw does not stay attached, and the packaging lacks required warnings.
Petzl America is recalling Nomic and Ergonomic ice climbing axes because the shaft can break at the handle during use. Twenty-six shaft breakages have been reported, with no injuries.
GLMZZ Fidget Magnet Ball Toy Sets are being recalled because they are high-powered magnets, violating the mandatory standard for toys and posing an ingestion hazard to children.
AirClub convertible bassinets are being recalled because the mechanism used to attach the product to an adult bed creates an opening between the bedside sleeper and the mattress, posing a fall hazard to infants.
Gillig is recalling 2023-2024 Low Floor transit buses because the rear weight placard may exceed tire ratings, increasing crash risk.
Cardinal Health is recalling Webcol Alcohol Prep pads because of non-sterility, with microbial contamination identified as Paenibacillus phoenicis. The FDA has classified this recall as Class I.
Volvo Trucks is recalling certain 2025-2026 VNL (4) vehicles because the service brake may take longer than expected to release, creating a crash risk and violating Federal Motor Vehicle Safety Standard 121.
Nissan is recalling 2026 Leaf vehicles because internal damage in the high voltage battery may cause a short circuit, increasing the risk of a fire.
GE Medical Systems is recalling Centricity Universal Viewer software versions 5.0 SP6 through 5.0 SP7.1 because user login credentials may be exposed on the local client workstation.
ConvaTec is recalling two lots of the EsteemBody Drainable Pouch, REF 423643, because the drainable large pouch may leak due to a manufacturing issue.
Somerset Therapeutics is recalling one lot of Dexamethasone Sodium Phosphate Injection after out-of-specification impurity results at product expiry during long term stability testing.
Baxter is recalling the Welch Allyn Spot Vision Screener VS100 on software version 3.2.0.1 because the display screen may unintentionally flicker, which may induce photosensitive seizure activity.
GE Medical Systems is recalling Centricity Universal Viewer software versions 6.0 through 6.0 SP10.4.1 because user login credentials may be exposed on the local client workstation.
Diagnostica Stago is recalling the STA Liatest D-Di kit after investigations confirmed a positive bias in D-dimer measurements throughout the entire analytical range.
ConvaTec is recalling one lot of the EsteemBody Drainable Pouch, REF 423653, because the drainable large pouch may leak due to a manufacturing issue.
Apotex is recalling two lots of Brimonidine Tartrate/Timolol Maleate Ophthalmic Solution for lack of assurance of sterility.
GE Medical Systems is recalling Centricity Universal Viewer software versions 7.0 through 7.0 SP2.0.1 because user login credentials may be exposed on the local client workstation.
Hologic is recalling one master lot of the Aptima HPV Assay because the product exhibits potential to generate either invalid or false negative results.