The Recall Desk

State

South Dakota product recalls

73,092 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 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

9901–9925 of 75776

  • HighNHTSA·24V668000·2024-09-10

    Freightliner and Western Star brake lights may fail during emergency braking

    Daimler Trucks is recalling certain Freightliner and Western Star trucks because brake lights may fail to illuminate during automatic emergency braking, increasing crash risk. Dealers will update software at no cost.

    Product
    FREIGHTLINER — FREIGHTLINER, WESTERN STAR 114SD, EM2, 57X, 47X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V661000·2024-09-10

    McLaren Recalls 2020-2023 GT Models Due to Hood Latch Defect

    McLaren is recalling 2020-2023 GT vehicles because the hood latch cable may have excessive tension, causing the hood to open unexpectedly and obstruct the driver's view.

    Product
    MCLAREN — MCLAREN GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V659000·2024-09-09

    Mercedes-Benz G 550 rear door latch defect poses safety risk

    Mercedes-Benz recalls 2019-2023 G 550 and 2019-2022 G63 AMG vehicles with faulty rear door latches that may fail to engage or prevent door operation, creating crash and injury risks.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G63, G 550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V658000·2024-09-09

    Mercedes-Benz Recalls 2024 GLC Models Due to Engine Carrier Weld Defect

    Mercedes-Benz is recalling 2024 GLC 300 and AMG GLC 43 vehicles because improper welds on the engine carrier may cause loss of vehicle control.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLC 300, AMG GLC43
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V655000·2024-09-06

    Phoenix Motorcars Transit Buses Recalled for Electrical System Fire Risk

    Phoenix Motorcars is recalling certain 2019-2021 800V Catalyst and 2020-2022 ZX5 transit buses. The vehicle software may cause the radiator fan electrical circuit to overheat, increasing fire risk.

    Product
    PROTERRA — PROTERRA ZX5, CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V656000·2024-09-06

    Airstream Recalls 2024 Trade Wind Trailers Due to Fire Risk

    Airstream is recalling 2024 Trade Wind travel trailers because the air conditioner soft start device may overheat, increasing the risk of a fire.

    Product
    AIRSTREAM — AIRSTREAM TRADE WIND
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E076000·2024-09-06

    Holley Sniper 2 EFI Throttle Body Recall for Fuel Leak Risk

    Holley is recalling 736 Sniper 2 EFI Throttle Bodies that may be missing a fuel plug, creating a risk of fuel leaks and fire.

    Product
    FUEL SYSTEM, GASOLINE:FUEL INJECTION SYSTEM:THROTTLEBODY/MANIFOLD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V653000·2024-09-05

    RAM 1500 Models Recalled for Anti-Lock Brake Software Malfunction

    Chrysler is recalling certain 2019, 2021-2024 RAM 1500 vehicles because a software malfunction in the ABS control module may disable the electronic stability control system, increasing crash risk.

    Product
    RAM — RAM 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E075000·2024-09-05

    Chrysler Recalls MOPAR ABS Modules for Electronic Stability Control Failure

    Chrysler is recalling MOPAR anti-lock braking system control modules used as replacement parts in certain Ram 1500 vehicles. A software malfunction may disable the electronic stability control system, increasing crash risk.

    Product
    ELECTRONIC STABILITY CONTROL (ESC):CONTROL MODULE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V652000·2024-09-05

    Instrument Panel Cluster May Fail in Jeep Wrangler Vehicles

    Jeep is recalling certain 2018-2024 Wrangler and 2020-2024 Gladiator vehicles because the instrument panel cluster may fail due to an internal short circuit, preventing drivers from seeing the speedometer and warning lights.

    Product
    JEEP — JEEP WRANGLER, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V654000·2024-09-05

    2024 Porsche Taycan Headlight Control Software Defect Recall

    Porsche is recalling 954 model year 2024 Taycan vehicles due to incorrect headlight control module software that may prevent parking lights from functioning when turn signals are activated, potentially reducing visibility and increasing crash risk.

    Product
    PORSCHE — PORSCHE TAYCAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24354·2024-09-05

    Delta Cycle Ceiling Hoists with Straps Recalled for Buckle Breakage Injury Risk

    Delta Cycle Corp is recalling ceiling hoists with straps because plastic buckles can break when holding kayaks, canoes, or other large objects. The company has received four incident reports, including one minor injury.

    Product
    Ceiling Hoists with Straps
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2726-2024·2024-09-04

    Stryker iBur Diamond Round surgical bur recalled for thermal overheating risk

    Stryker iBur 4.0mm Diamond Round surgical burs may reach temperatures higher than specified, potentially causing thermal injury or tissue damage during bone-cutting procedures. Approximately 1,706 affected units have been distributed worldwide.

    Product
    Stryker iBur 4.0mm Diamond Round, Distal Bend- intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology; and
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2919-2024·2024-09-04

    BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Quality Concern

    Beaver Visitec International is recalling 227 units of BVI CustomEyes Procedure Packs containing syringes from Sol-Millennium Medical due to a quality concern affecting those syringes.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001838;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0646-2024·2024-09-04

    Prescription Ibuprofen Tablets Recalled for Excessive Unknown Impurities

    Dr. Reddy's Laboratories is recalling IBU Ibuprofen 400 mg prescription tablets due to impurity levels exceeding specifications. The recall affects 14,940 bottles distributed nationwide in the USA and Puerto Rico.

    Product
    IBU — IBU (IBUPROFEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2727-2024·2024-09-04

    Stryker iBur surgical burs recalled due to overheating risk

    Stryker Corporation recalls iBur 3.0mm surgical burs used in neurosurgery, spinal, and ENT procedures due to potential overheating at the bur-shank interface. The heat risk may cause tissue damage requiring medical intervention.

    Product
    Stryker iBur 3.0mm Coarse Diamond Round, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngolo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1756-2024·2024-09-04

    NOW Real Foods Brazil Nuts Recalled for Mold and Yeast Contamination

    NOW Real Foods Whole & Unsalted Raw Brazil Nuts are recalled due to high levels of mold, yeast, and microbial contamination. The recall affects 7,854 units distributed nationwide and to Singapore.

    Product
    NOW Real Foods Whole & Unsalted Raw Brazil Nuts 12oz. bag UPC 733739070128
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0644-2024·2024-09-04

    Prescription Ibuprofen Recalled Due to Failed Impurity Specifications

    Dr. Reddy's Laboratories is recalling IBU (Ibuprofen) 800 mg prescription tablets nationwide due to failed quality specifications. Testing found unknown impurities exceeding acceptable limits.

    Product
    IBU — IBU (IBUPROFEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2838-2024·2024-09-04

    BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled

    Beaver Visitec International recalls BVI CustomEyes Procedure Packs containing Sol-M brand syringes due to manufacturer's voluntary recall. 130 units distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001020;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2864-2024·2024-09-04

    BVI CustomEyes Procedure Packs with Sol-M Syringes Recalled

    Beaver Visitec International, Inc. is recalling BVI CustomEyes Procedure Packs containing Sol-M manufactured syringes. The voluntary recall affects approximately 1,629 units distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001376;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2730-2024·2024-09-04

    Stryker iBur surgical bur may overheat during bone-cutting procedures

    Stryker iBur 3.0mm Diamond Match Head surgical cutting tools may reach temperatures exceeding safe operating limits during bone surgery, potentially causing thermal tissue injury. About 2,507 units worldwide are affected.

    Product
    Stryker iBur 3.0mm Diamond Match Head, Distal Bend - intended to cut bone in the following manner: drilling, reaming, decorticating, shaping, dissecting, shaving, and smoothing for the following medical applications: Neuro; Spine; Ear, Nose, and Throat (ENT)/ Otorhinolaryngology
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2839-2024·2024-09-04

    BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Recall

    Beaver Visitec International is recalling BVI CustomEyes Procedure Packs because they contain Sol-Millennium Medical syringes that are subject to a manufacturer recall. A total of 103 units were distributed nationwide.

    Product
    BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001025;
    Category
    Medical Device
    Distribution
    Distributed nationwide