The Recall Desk

State

South Dakota product recalls

73,106 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 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

12001–12025 of 75790

  • HighFDA (Devices)·Z-1508-2024·2024-04-17

    Nucleic Acid Isolation Device Recall: EZ2 Connect MDx-IVD Heater Failure

    Qiagen Sciences is recalling 168 units of the EZ2 Connect MDx-IVD nucleic acid isolation device due to insufficient welding that causes heater cable embrittlement and device malfunction, resulting in sample loss during testing.

    Product
    EZ2 Connect MDx-IVD Designed to perform automated isolation and purification of nucleic acids in molecular diagnostic and/or molecular biology applications. Model Number: 9003230
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V272000·2024-04-17

    Forest River Travel Trailers LED Backlight Circuit Board Fire Risk

    Forest River and Dynamax are recalling multiple 2018–2024 travel trailer models due to LED backlight circuit boards in cooktop ranges that may overheat and create a fire risk. Dealers will disconnect and remove the LED backlight wiring at no charge.

    Product
    FOREST RIVER — FOREST RIVER, DYNAMAX IBEX, DX3, CEDAR CREEK, WILDCAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1516-2024·2024-04-17

    PEG feeding tube with blocked connector may impede placement procedure

    Boston Scientific's EndoVive 20Fr PEG Kit may have a blocked connector that prevents the guidewire from advancing during placement, potentially causing complications including bleeding and aspiration.

    Product
    EndoVive 20Fr Push Standard PEG Kit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00568211
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1482-2024·2024-04-17

    RayStation Software Use Error Could Cause Incorrect Radiation Dose Calculations

    RayStation radiation therapy planning software versions 8B through 2024A contain a use error that can incorrectly select silicon material for silicone gel polymer implant dose calculations, potentially resulting in incorrect radiation doses.

    Product
    RayStation Software Version Numbers version numbers 8B, 9A, 9B, 10A, 10B, 11A, 11B, 12A, 12B, 2023B, 2024A including some service packs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1497-2024·2024-04-17

    Acetabular Bearing Components Recalled for Marketing Without FDA Clearance

    Synovo Production is recalling 1,681 acetabular bearing components that were marketed without FDA clearance.

    Product
    ACETABULAR BEARING (xx)MM I.D X (xx) O.D. UHMWPE 1020, STERILEEO, Reference Numbers: 01-02-4254 01-02-4456 01-02-4558 01-02-4760 01-02-4962 01-02-5164 01-02-5266
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1518-2024·2024-04-17

    da Vinci SP Surgical System Patient Cart Welds May Fail

    Intuitive Surgical recalled 53 da Vinci SP Surgical System Patient Carts due to inadequate welds in the instrument arm joints. These welds may cause tissue injuries, conversion to open surgery, or user pinching injuries.

    Product
    Patient Cart, Part: 380601, a component of the da Vinci SP Surgical System, Model: SP1098
    Category
    Medical Device
    Distribution
    21 states
  • HighNHTSA·24V275000·2024-04-17

    Lexus LS Air Bag Sensor May Fail to Detect Front Passenger

    Toyota is recalling certain 2018–2021 Lexus LS and LS Hybrid vehicles with the Executive Package because the front passenger seat occupant sensor may fail to detect a passenger, risking improper air bag deployment in a crash.

    Product
    LEXUS — LEXUS LS, LS HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1513-2024·2024-04-17

    EndoVive 20Fr Push Safety PEG Kit Recall Due to Blocked Lumen Risk

    Boston Scientific is recalling the EndoVive 20Fr PEG feeding kit due to blockage in the barb connector that can prevent proper placement. The blockage may lead to prolonged procedures, bleeding, gastric leakage, and aspiration risk.

    Product
    EndoVive 20Fr Push Safety PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509011
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1514-2024·2024-04-17

    PEG Feeding Tube Kit Recalled for Blocked Lumen Preventing Guidewire Advancement

    Boston Scientific is recalling 572 EndoVive PEG feeding tube kits due to a blocked lumen in the barb connector that may prevent guidewire advancement during placement, potentially requiring device exchange and increasing risk of complications.

    Product
    EndoVive 20Fr Push Standard PEG Kit w/ENFit (Box 2)-Indicated for enteral nutrition directly into the stomach in both pediatric and adult patients who are unable to consume nutrition by conventional means. UPN: M00509051
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0438-2024·2024-04-17

    FDA Recalls Lansoprazole Delayed-Release Capsules for Manufacturing Practice Deviations

    NATCO Pharma Limited is voluntarily recalling 30 bottles of Lansoprazole 15 mg delayed-release capsules due to Current Good Manufacturing Practice deviations. The product was distributed nationwide in the United States.

    Product
    Lansoprazole Delayed-Release Capsules USP, 15 mg, Acid reducer 24 Hour, Treats Frequent Heartburn, 14 capsules per bottle, Manufactured by: Natco Pharma Limited Kothur- 509 228, India, Distributed by: Rising Pharma Holdings, Inc. East Brunswick, NJ. 08816. NDC 16571-742-41
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V270000·2024-04-16

    Kawasaki Recalls 2024 Z900RS Motorcycles Due to Front Tire Defect

    Kawasaki is recalling 2024 Z900RS motorcycles because a manufacturing error may cause front tire blistering, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI ZR900C, ZR900E, ZR900N
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V271000·2024-04-16

    2023 Kia Niro EV Differential Bolt Recall: Loss of Drive Power Risk

    Kia is recalling certain 2023 Niro EV vehicles because differential gear bolts may not be properly tightened, potentially causing loss of drive power or differential lock-up, which can increase crash risk.

    Product
    KIA — KIA NIRO EV, EV9
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V265000·2024-04-12

    Forest River Recalls 2024 Cardinal and Wildcat Fifth Wheel Trailers

    Forest River is recalling 2024 Cardinal and Wildcat fifth wheel trailers because the rear towing hitch may be used without locking the turning point, increasing crash risk.

    Product
    FOREST RIVER — FOREST RIVER CARDINAL, WILDCAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V268000·2024-04-12

    Outdoors RV Recalls Titanium Trailers Due to Cooktop Fire Risk

    Outdoors RV is recalling 2022-2024 Titanium trailers because the cooktop LED backlight circuit board may overheat, increasing the risk of a fire.

    Product
    OUTDOORS RV — OUTDOORS RV TITANIUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V267000·2024-04-12

    Ford Bronco Sport Control Module Failure May Disable Drive Power

    Ford is recalling Bronco Sport and Maverick models due to control module defects that may fail to detect low battery charge, potentially disabling drive power and increasing crash risk. Dealers will provide free recalibration.

    Product
    FORD — FORD BRONCO SPORT, MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V266000·2024-04-12

    2024 Ford Maverick Tire Pressure and Capacity Label Recall

    Ford is recalling certain 2024 Maverick vehicles due to incorrect tire and loading information labels. These incorrect labels may result in vehicle overload and increase crash risk.

    Product
    FORD — FORD MAVERICK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E032000·2024-04-12

    Ford Recalls Bronco Sport Hood Scoops Due to Detachment Risk

    Ford is recalling certain Bronco Sport hood scoops that may detach while driving, posing a risk of windshield damage or road hazards.

    Product
    STRUCTURE:BODY:HOOD recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24199·2024-04-11

    Zipline Kits Recalled Due to Cable-Breaking Fall Hazard

    Jugader Zipline Kits sold on Amazon.com from March 2020 through June 2023 are recalled because the stainless-steel cable can break, causing falls. The manufacturer has received 20 reports of cable breakage resulting in nine injuries.

    Product
    Zipline Kits
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24743·2024-04-11

    Matrix T1 and T3 Commercial Treadmills Fire Hazard Expansion Recall

    Johnson Health Tech North America is expanding its recall of Matrix T1 and T3 Series commercial treadmills due to a fire hazard from loose power cords. About 9,700 additional units are affected.

    Product
    Matrix T1 and T3 Series Commercial Treadmills
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V263000·2024-04-11

    Keystone Recalls 2024 Trailers Due to Axle Frame Contact Risk

    Keystone RV is recalling 214 specific 2024 trailer models because the suspension equalizer may allow the axle to contact the frame, increasing crash risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN HAMPTON, RETREAT, ASPEN TRAIL LOFT, RESIDENCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24192·2024-04-11

    BRS Liquid Fuel Bottles Recalled for Non-Child-Resistant Closure Risk

    About 1,600 BRS portable liquid fuel bottles with non-child-resistant closures have been recalled due to risk of burn and poisoning to children. The closure does not meet requirements of the Children's Gasoline Burn Prevention Act.

    Product
    BRS Liquid Fuel Bottles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24193·2024-04-11

    Red Land Cotton Recalls Quilts and Shams Due to Laceration Hazard

    Red Land Cotton is recalling approximately 17,400 quilts and quilted shams sold on Amazon.com because pieces of broken needles inside the products pose a laceration hazard. The company has received three reports of consumers being jabbed by sharp metal needles.

    Product
    Red Land Cotton "Quilts" and "Quilted Shams"
    Category
    Consumer Product
    Distribution
    Distributed nationwide