State
73,382 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 73,382 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Calico Cottage Inc is recalling Salted Nut Roll Pre-Made Fudge nationwide because the peanut butter ingredient is potentially contaminated with Salmonella.
Albertsons Companies LLC is recalling Mini Peanut Butter Cream Pies sold at Haggen stores across 32 states due to potential Salmonella contamination. Consumers should not consume the affected pies.
Olympus Corporation recalls a single colonovideoscope model CF-H180AL because an incorrect camera unit was installed, causing narrower viewing angle and potential device protrusion that could injure tissue. No injuries have been reported.
Teva Pharmaceuticals is recalling Tretinoin Capsules (10 mg) nationwide due to failed dissolution specifications that may affect medication effectiveness. Patients should contact their pharmacist or doctor to confirm if their prescription is affected.
Sun Pharmaceutical recalls 97,450 vials of Testosterone Cypionate Injection nationwide due to manufacturing deviations that could cause out-of-specification impurities.
Sun Pharmaceutical is recalling approximately 47,500 vials of Testosterone Cypionate Injection due to a manufacturing deviation that may have affected product sterility.
Red Button Vintage Creamery Canadian Vanilla Ice Cream was distributed nationwide with undeclared almond allergen due to packaging mix-up. Consumers with tree nut allergies should not consume this product.
Bard Peripheral Vascular Inc is recalling certain catheter drainage kits that may contain an 8 Fr needle instead of the correct 6 Fr needle. The incorrect needle size could cause tissue injury during patient care.
EarthLab Inc is recalling Wise Woman Herbals Standardized Kava Glycerite due to high yeast and mold counts detected during microbial testing. The affected product was distributed nationwide.
Vi-Jon's 70% isopropyl alcohol bottles may leak when squeezed or tilted due to defects in the bottle neck finish. Over 3 million bottles with various lot numbers were distributed nationwide.
Sun Pharmaceutical is recalling Clonazepam Orally Disintegrating Tablets (0.125mg) due to manufacturing defects where oversized tablets were found. The affected lot (MHC1430A, exp. 09/2023) was distributed nationwide.
Beaver Visitec International recalled 660 units of BVI Wet-Field Eraser surgical devices after discovering boxes labeled with one tip configuration contained a different tip design. This mismatch could affect surgical precision and hemostasis control.
KZRV is recalling 2021 Escape travel trailers because the tire placard lists incorrect information, which can lead to overinflated tires and increased crash risk.
Maquet Cardiovascular recalls INTERGARD Woven Vascular Grafts with incorrect labeling. Units labeled as 8 mm diameter instead contained 32 mm diameter grafts.
CardioTek EP-TRACER Software V2.x is recalled because it failed electrical safety testing for insulation. The 146 affected units were distributed worldwide.
Olympus is recalling 8 EVIS EXERA II gastrointestinal videoscopes (Model GIF-HQ190) because an incorrect rubber component may have been installed during repair. The incorrect part does not meet the device's design specifications.
EarthLab Inc is recalling Wise Woman Herbals Kava Capsules nationwide due to microbial contamination. Quality testing found yeast and mold counts that exceeded acceptable levels.
EarthLab Inc is recalling Wise Woman Herbals Sleepytime Glycerite due to elevated yeast and mold levels detected in microbial testing. Consumers should discontinue use.
Mayne Pharma is recalling 1,440 cartons of Clonidine transdermal patches nationwide due to an out-of-specification defect in the release liner that could affect proper drug delivery.
Creminelli Fine Meats is recalling approximately 4,207 pounds of mini parmesan salami sticks because the product contains an undeclared egg allergen.
Custom Fire Apparatus is recalling one 2018 Peterbilt 348 fire truck because steering arm fasteners may fail, potentially causing loss of steering control.
Daimler Trucks North America is recalling 2022-2023 FCCC MT50E walk-in vans because a broken electronic axle parking pawl may cause vehicle rollaway.
Hyundai is recalling 2017-2018 Ioniq Hybrid and Plug-in Hybrid vehicles because a power relay assembly may overheat, increasing the risk of a fire.
Hyundai is recalling 2020-2022 Venue vehicles because the front seat belt pretensioners may explode when deployed in a crash, potentially projecting metal fragments at occupants.
Airstream is recalling 2022 Caravel, Flying Cloud, Globetrotter, International, and Pottery Barn travel trailers because a bearing washer may crack, causing the hub to separate from the axle.