The Recall Desk

State

South Dakota product recalls

73,096 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 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10526–10550 of 75780

  • HighNHTSA·24V572000·2024-08-01

    2021 Jeep Wrangler and Gladiator powertrain control software recall

    Chrysler is recalling certain 2021 Jeep Wrangler and Gladiator vehicles due to a powertrain control module software defect that may cause engine stall, resulting in loss of drive power and increased crash risk.

    Product
    JEEP — JEEP GLADIATOR, WRANGLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V573000·2024-08-01

    2023 Dodge Challenger: Rear Seat Back May Not Lock in Upright Position

    The left rear seat back in certain 2023 Dodge Challengers may not lock in the upright position, increasing the risk of injury in a crash. Dealers will inspect and adjust the seat latch free of charge.

    Product
    DODGE — DODGE CHALLENGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V577000·2024-08-01

    Jayco Recalls 2024-2025 Entegra Motorhomes Due to Battery Cable Fire Risk

    Jayco is recalling 2024-2025 Entegra motorhomes because improperly sized or installed battery cables may overheat or short, increasing the risk of a fire.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE, REATTA XL, ANTHEM, ASPIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24332·2024-08-01

    Brompton T-Line Foldable Bicycles Recalled for Fall Hazard

    Brompton T-Line Foldable Bicycles are recalled because loose steerer clamp bolts can cause misalignment between the handlebar and front wheel, risking loss of steering control and falls. About 1,080 units are affected.

    Product
    Brompton T-Line Foldable Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24331·2024-08-01

    RH Baby & Child Jeune Cribs Recalled for Choking Hazard

    RH Baby & Child is recalling about 480 Jeune French Contemporary Upholstered Panel Cribs because cylindrical metal inserts in the wooden frame can become loose and detach, posing a choking hazard to infants.

    Product
    Jeune French Contemporary Upholstered Panel Cribs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24328·2024-08-01

    LED Light-up Jelly Ring Toys Recalled for Battery Ingestion Hazard

    Attom Tech is recalling about 4,100 LED light-up jelly ring toys sold on Amazon because the button cell batteries inside can be easily accessed and swallowed by children, posing a risk of serious internal injury and death.

    Product
    LED Light-up Jelly Ring Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V569000·2024-08-01

    Thomas Built Buses Recalls 2024-2025 Saf-T-Liner C2 Models for Fire Risk

    Daimler Trucks North America is recalling 2024-2025 Thomas Built Buses Saf-T-Liner C2 and C2 Jouley school buses because an improperly installed air conditioning ground cable may overheat and cause a fire.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2 JOULEY, SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24329·2024-08-01

    ECHO Gas-Powered Backpack Blowers Recalled Due to Fire Hazard

    ECHO Inc. is recalling about 3,900 gas-powered backpack blowers due to a fuel supply line that can leak gas, creating a fire hazard. No injuries have been reported.

    Product
    ECHO gas-powered backpack blowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24324·2024-08-01

    Beberoad New Moon Travel Bassinets Recalled for Fall Hazard

    Beberoadlove is recalling about 1,940 New Moon Travel Bassinets because they lack a required stand and can fall from elevated surfaces, violating federal safety regulations for infant sleep products. No injuries have been reported.

    Product
    Beberoad New Moon Travel Bassinets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24326·2024-08-01

    Peace Sports Youth ATVs Recalled for Safety Violations and Injury Risk

    Peace Industry Group is recalling about 1,000 Peace Sports Youth All-Terrain Vehicles due to violations of federal ATV safety standards. The ATVs have defective handlebars, faulty parking brakes, missing reflectors, and footguards that pose risks of laceration, amputation, and collision.

    Product
    Peace Sports Youth All-Terrain Vehicles (ATVs)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24325·2024-08-01

    Papablic Archie Infant Swings Recalled for Suffocation Hazard

    Papablic Archie Infant Swings (model PAPABLIC61A) pose a suffocation risk because they are designed for infant sleep with an incline angle greater than 10 degrees, violating federal safety regulations. Consumers should stop using them immediately.

    Product
    Papablic Archie Infant Swings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24327·2024-08-01

    Origin 21 Wall Mirrors Recalled for Fall and Laceration Hazards

    Lowe's has recalled about 27,400 Origin 21 oval and rectangle black framed wall mirrors because they can detach from their metal hanging plates and fall, creating laceration and impact hazards. The company has received 15 reports of separation with no injuries yet reported.

    Product
    Origin 21 Oval and Rectangle Black Framed Wall Mirrors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24330·2024-08-01

    Avocado Organic Cotton Mattress Pad Protectors Recalled for Fire Hazard

    About 55,480 Avocado Organic Cotton Mattress Pad Protectors are being recalled because they violate the federal flammability regulation for mattress pads, posing a fire hazard. No injuries have been reported.

    Product
    Avocado Organic Cotton Mattress Pad Protectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24V574000·2024-08-01

    2023 Dodge Charger Seat Back Latch May Not Lock Properly

    The left rear seat back in certain 2023 Dodge Charger vehicles may not lock in the upright position. This creates a risk of injury in a crash.

    Product
    DODGE — DODGE CHARGER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·24V575000·2024-08-01

    2024 Chevrolet Malibu Vehicles Recalled for Wrong Owner Manual

    General Motors is recalling 2024 Chevrolet Malibu vehicles that may have an incorrect owner's manual. The wrong manual could contain inaccurate vehicle safety information.

    Product
    CHEVROLET — CHEVROLET, CADILLAC MALIBU, XT4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V568000·2024-07-31

    Jayco Recalls 2025 Entegra Cornerstone Motorhomes Due to Fire Risk

    Jayco is recalling 2025 Entegra Cornerstone motorhomes because inadequate fuse protection on chassis batteries increases the risk of a fire.

    Product
    ENTEGRA — ENTEGRA CORNERSTONE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2409-2024·2024-07-31

    NIM Vital Nerve Monitoring Systems Recalled for False Negative Risk

    Medtronic Xomed is recalling NIM Vital Nerve Monitoring systems because they may fail to detect nerve damage or dysfunction. Approximately 7,804 units were distributed worldwide.

    Product
    NIM Vital Nerve Monitoring systems (all serial numbers manufactured) with NIM Vital System versions: v1.0.0, v1.1.1, v1.3.2, v1.4.3. NIM Vital Nerve Integrity Monitor with below product descriptions. 1. CONSOLE NIM4CM01 NIM 4.0, Model Number: NIM4CM01. 2. CONSOLE NIM4CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2438-2024·2024-07-31

    Sensis Vibe diagnostic systems software crash during event documentation

    Siemens Sensis Vibe diagnostic systems may crash when using documentation features during once-per-study event reporting. Three systems are affected; no injuries reported.

    Product
    Sensis Vibe systems with software version VD15B in combination with Sensis High End Server -Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology as wel
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2437-2024·2024-07-31

    Perfusor Space Syringe Pump Recalled for Monoject Syringe Incompatibility Risk

    B Braun's Perfusor Space infusion pump may be incompatible with Cardinal Health Monoject syringes affected by manufacturing changes, creating risks of overdose, underdose, and delayed therapy.

    Product
    Brand Name: Perfusor Space Product Name: Perfusor Space Syringe Pump, Non-Wireless Model/Catalog Number: 8713032U Product Description: Perfusor Space Syringe Pump, Non-Wireless, Infusion Pump, 1 each Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2427-2024·2024-07-31

    Medtronic A610 Clinician Programmer pocket adaptors limited to head-only MRI

    Medtronic recalled A610 Clinician Programmer software and pocket adaptors (Models 64001, 64002) due to MRI safety restrictions. Patients with these implants are limited to head-only MRI procedures.

    Product
    A610 Clinician Programmer (CP) Software Application (app) with the following versions: Version 2.0.x (2.0.4584, 2.0.4594, 2.0.4605, 2.0.4630, and 2.0.4648), Version 3.0.x (3.0.1057, 3.0.1062, 3.0.1081, and 3.0.1098), Version 4.0.x (4.0.1052). Includes the below product descripti
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2432-2024·2024-07-31

    Abbott Infinity 7 Implantable Pulse Generators Recalled for Potentially Shortened Service Life

    Abbott is recalling 1198 Infinity 7 Implantable Pulse Generators due to potentially incorrect service life indicators and end-of-service dates in product labeling, which could result in loss of therapy.

    Product
    Abbott Infinity 7, Implantable Pulse Generator, REF: 6663, SterileEO, Rx Only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2441-2024·2024-07-31

    Sensis Vibe medical diagnostic system software crashes during documentation events

    A software issue in certain Siemens Sensis Vibe diagnostic systems may cause the application to crash when documentation features are used during clinical reporting events.

    Product
    Sensis Vibe systems with software version VD15B-Intended to be used as a diagnostic and administrative tool supporting hemodynamic catheterizations and/or electrophysiology studies, for cardiac as well as interventional Radiology as well as surgical studies. Equipped by modules,
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2435-2024·2024-07-31

    Perfusor Space syringe pump recalled for Cardinal Health syringe incompatibility

    B Braun is recalling Perfusor Space syringe pumps because manufacturing changes to Cardinal Health Monoject syringes may cause incompatibility, resulting in dosing errors or delayed treatment.

    Product
    Brand Name: Perfusor Space Product Name: Perfusor PCA Syringe Pump Model/Catalog Number: 8713080U Product Description: Perfusor¿ Space Syringe Pump, Infusion Pump, 1 each Component: N/A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2423-2024·2024-07-31

    Medtronic TourniKwik Tourniquet Set Recalled for Incorrect Component

    Medtronic is recalling 636 units of TourniKwik Tourniquet Sets due to incorrect components placed in four manufactured lots. Distribution includes the US states of Minnesota, Massachusetts, Utah, California, Florida, Japan, and Slovenia.

    Product
    TourniKwik Tourniquet Set (CFN 79012)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2428-2024·2024-07-31

    Beckman Coulter Clinical Reagent Recalled Due to Incorrect Lipemia Check Settings

    Beckman Coulter has recalled 13,565 units of IGM clinical reagent due to incorrect lipemia check settings that may produce false low results or report high results as normal. Affected units were distributed worldwide.

    Product
    Beckman Coulter, REF: OSR61173, IGM 4x14 mL R1, 4x11 mL R2
    Category
    Medical Device
    Distribution
    Distributed nationwide