The Recall Desk

State

South Dakota product recalls

73,219 recalls have nationwide distribution and so reach South Dakota. 2,684 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total
2,684
Critical
401
Severe
567
Most recent
2026-09-23

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.

These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,219 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

16951–16975 of 75903

  • SevereNHTSA·23V246000·2023-04-06

    Prevost Recalls 2023 X3-45 VIP Motor Coaches Due to Fire Risk

    Prevost is recalling 2023 X3-45 VIP motor coaches because a missing grommet allows electrical cables to chafe, potentially causing a short circuit and fire.

    Product
    PREVOST — PREVOST X3-45 VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V253000·2023-04-06

    2023 BMW X5 Head Restraints May Fail in Crash

    BMW is recalling approximately 235 certain 2023 X5 vehicles with defective second-row head restraints that may not properly restrain occupants during a crash, violating federal safety standards.

    Product
    BMW — BMW X5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·23174·2023-04-06

    Mammut Avalanche Shovels Recalled for Spring Locking Mechanism Failure

    Mammut Sports Group is recalling Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels because the spring locking mechanism can fail during emergency excavation, posing risk of injury or death.

    Product
    Alugator Ride 3.0 Hoe and Alugator Ride SE avalanche shovels
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V245000·2023-04-06

    Prevost Recalls 2023 X3-45 Motor Coaches Due to Electrical Fire Risk

    Prevost is recalling 2023 X3-45 and X3-45 VIP motor coaches because an insufficient grommet allows electrical cables to chafe, potentially causing a short circuit and fire.

    Product
    PREVOST — PREVOST X3-45 VIP, X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V248000·2023-04-06

    Navistar Recalls International Buses Due to HVAC Wiring Fire Risk

    Navistar is recalling 2016-2020 International and IC Bus models because an HVAC wiring terminal may overheat, increasing the risk of a fire.

    Product
    INTERNATIONAL — INTERNATIONAL, IC BUS TRANSTAR, DURASTAR, PROSTAR, LONESTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V252000·2023-04-06

    2022–2023 Land Rover Range Rover Seat Frame Defect Recall

    Jaguar Land Rover North America is recalling certain 2022–2023 Land Rover Range Rover vehicles because the second-row left seat frame may have been insufficiently welded and may not adequately secure occupants during crashes or sudden braking.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·23742·2023-04-06

    Monti Kids Basket with Balls Toys Recalled for Choking Hazard

    Monti Kids is recalling Basket with Balls toys sold in subscription boxes because the blue crocheted ball's sewn swirls can separate and expose small parts, creating a choking hazard for young children.

    Product
    Basket with Balls toys sold with Monti Kids Tummy-Time, 4-6M Play and Early Gross Motor subscription boxes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·23175·2023-04-06

    IKEA Recalls BLÅVINGAD Fishing Games Due to Choking Hazard

    IKEA is recalling about 25,000 BLÅVINGAD fishing games because a small metal rivet in a wooden play piece can come loose and pose a choking hazard to young children. Four incidents have been reported globally, with none in the U.S. requiring medical attention.

    Product
    BLÅVINGAD fishing games
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·23176·2023-04-06

    BISSELL Cordless Wet Dry Vacuums Recalled for Fire Hazard

    BISSELL is recalling about 2,000 Cordless Multi-Surface Wet Dry Vacuums (models 2551R and 25518) because the battery pack circuit board can overheat and smoke, creating a fire hazard. No injuries have been reported.

    Product
    BISSELL® Cordless Multi-Surface Wet Dry Vacuums Models 2551R and 25518
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V243000·2023-04-05

    New Flyer Recalls 2023 XD60 and XDE60 Buses for ABS Failure

    New Flyer is recalling 2023 XD60 and XDE60 buses because the anti-lock brake system may lose power during hard braking, increasing crash risk.

    Product
    NEW FLYER — NEW FLYER XD60, XDE60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V242000·2023-04-05

    Maserati Recalls 2023 MC20 Cielo for Windshield Frame Bonding Defect

    Maserati is recalling 2023 MC20 Cielo vehicles because insufficient windshield frame bonding could allow the frame to detach in a crash, increasing injury risk.

    Product
    MASERATI — MASERATI MC20 CIELO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1315-2023·2023-04-05

    Disposable Tourniquet Cuffs Recalled Due to Pressure Failure

    Over 127,000 disposable tourniquet cuffs are being recalled because they may fail to achieve or maintain pressure during surgery due to fabric tearing or O-ring defects, risking operative bleeding and hemorrhage.

    Product
    Color Cuff Single Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-135; Color Cuff Dual Port, Single Bladder 30 (Royal Blue) Quick Connect, REF: 5921-030-235; Color Cuff Single Port, Single Bladder 34 (Purple), Quick Connect, REF…
    Category
    Medical Device
    Distribution
    50 states
  • HighFDA (Drugs)·D-0533-2023·2023-04-05

    Dabigatran Etexilate Drug Recalled Due to N-nitroso Impurity

    Ascend Laboratories is recalling 13,560 bottles of Dabigatran Etexilate 75 mg capsules nationwide because testing detected N-nitroso-dabigatran impurity levels above acceptable limits. The issue stems from a manufacturing quality control deviation.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1312-2023·2023-04-05

    Defibtech DDU-100 Lifeline AED Recalled for Untested Component Risk

    Defibtech is recalling 29 units of the DDU-100 Lifeline AED due to an untested component that could cause device failure. The affected device may not deliver therapy if a malfunction occurs.

    Product
    DDU-100 Lifeline Automated External Defibrillator (AED)-Indicated for use on victims of sudden cardiac arrest
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1285-2023·2023-04-05

    Dental Implant Titanium Base Recalled for Stability and Fracture Risk

    Preat Corp is recalling Neodent GM X 6mm titanium base components due to a dimensional defect causing vertical movement. This instability may lead to abutment fracture and potential ingestion of dental materials by patients.

    Product
    Neodent GM X 6mm Engaging Titanium Base, REF: 9007162
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0475-2023·2023-04-05

    Calcitonin Salmon Nasal Spray Recalled for Out-of-Specification Impurities and Low Potency

    Endo Pharmaceuticals is recalling Calcitonin Salmon Nasal Spray due to out-of-specification impurities and subpotent drug content. Affected lots distributed nationwide have expiration dates ranging from March 2023 to March 2025.

    Product
    CALCITONIN SALMON — CALCITONIN SALMON (CALCITONIN SALMON)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1300-2023·2023-04-05

    PCRopsis Reagent RVD-RT in vitro diagnostic kit recall for misleading labels

    Entopsis, Inc. is recalling PCRopsis Reagent RVD-RT diagnostic kits due to misleading label statements that could affect proper use and test interpretation.

    Product
    PCRopsis Reagent RVD-RT, IVD: a) 1 mL, REF 78378001; b) 25 mL, REF 78378025; c) 100 mL, REF 78378100; Extraction-free PCR at room temperature; nucleic acid extraction from a variety of biological samples
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0687-2023·2023-04-05

    Almost Famous Popcorn Poppy Chow recalled for undeclared peanut allergen

    Rieckhoff Family Businesses is recalling Almost Famous Popcorn Poppy Chow because peanuts are listed in ingredients but omitted from the allergen statement. Consumers with peanut allergies may be at serious risk.

    Product
    Almost Famous Popcorn Poppy Chow, 9.9 oz bag (UPC 8 5001151513)
    Category
    Food
    Distribution
    13 states
  • HighFDA (Devices)·Z-1290-2023·2023-04-05

    GaGa Pro Class IV Laser Projectors Recalled for FDA Compliance Failure

    GaGa Pro Lighting Equipment Co. manufactures Class IV Laser Light Show projectors that are being recalled due to non-compliance with FDA's Performance Standard for laser products. Eleven units distributed nationwide are affected.

    Product
    GaGa Pro Lighting Equipment Co. Ltd. manufactures Class IV Laser Light Show (LLS)projectors for the purposes of demonstration and entertainment.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0534-2023·2023-04-05

    Prescription Drug Dabigatran Etexilate Recalled for Excess Nitrosamine Impurity

    Ascend Laboratories is recalling 12,804 bottles of Dabigatran Etexilate 150mg capsules nationwide due to detection of N-nitroso-dabigatran (NDAB) impurity levels above the Acceptable Daily Intake limit caused by manufacturing process deviations.

    Product
    DABIGATRAN ETEXILATE — DABIGATRAN ETEXILATE (DABIGATRAN ETEXILATE)
    Category
    Drug
    Distribution
    Distributed nationwide