The Recall Desk

State

South Dakota product recalls

73,118 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 73,118 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13351–13375 of 75802

  • SevereNHTSA·24V014000·2024-01-11

    GM Recalls 2022 BrightDrop EV600 Vehicles Due to Fire Risk

    General Motors is recalling 2022 BrightDrop EV600 vehicles because the front-drive unit may leak oil, creating a risk of engine compartment fire.

    Product
    BRIGHTDROP — BRIGHTDROP EV600
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24080·2024-01-11

    Daikin Evaporator Coil Drain Pans Expansion Recall Due to Fire Hazard

    Daikin Comfort Technologies Manufacturing is expanding its recall of evaporator coil drain pans that can overheat, melt, and deform, creating a fire hazard. The expansion includes about 3,600 additional units manufactured between January 2019 and February 2020 that were incorrectly marked with a 2018 serial number.

    Product
    Evaporator coil drain pans
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E003000·2024-01-11

    SVI Trucks Recalls Command Light Towers Due to Electrical Fire Risk

    SVI Trucks is recalling Command Light Towers and Traffic Flowboards with specific Weldon nodes because a wiring failure could cause an electrical fire.

    Product
    ELECTRICAL SYSTEM:WIRING recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V015000·2024-01-11

    2004-2023 Altec Aerial Devices recalled for engine compartment cable fire risk

    Altec is recalling certain 2004-2023 AT Series aerial devices because cables in the engine compartment may contact the hood, damaging the cables and causing a short circuit that increases fire risk. Free repair available through Altec.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24078·2024-01-11

    Millions of New Age Furniture Tip Restraint Kits Recalled for Tip-Over and Entrapment Hazard

    Plastic New Age furniture tip restraint kits can break or become brittle, allowing anchored clothing storage units to detach and tip over, creating a hazard to children. Consumers should check manufacture dates and contact Alliance4Safety for free replacements.

    Product
    New Age Industries ("New Age") Furniture tip kits or tip restraints
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24081·2024-01-11

    Scout Kid's Bike Helmets Recalled for Head Injury Risk

    Retrospec is recalling Scout model kid's bike helmets due to inadequate impact protection that violates the federal safety regulation for bicycle helmets. About 72,000 units sold between February 2019 and March 2023 are affected.

    Product
    Scout Kid's Bike Helmets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24082·2024-01-11

    Justin Boots Keaven WP Met Guard Work Boots Recalled Due to Missing Metatarsal Guard

    Boot Royalty is recalling about 3,200 Justin Boots Keaven WP Met Guard Work Boots (Model SE4570) because the metatarsal guard may be missing, creating a crush hazard to the wearer's feet. One injury has been reported.

    Product
    Justin Boots Keaven WP Met Guard Work Boots Model SE4570
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0594-2024·2024-01-10

    Tracheostomy care sets recalled for sterility assurance failure

    Busse Hospital Disposables is recalling tracheostomy care kits due to failed sterility assurance. The affected product cannot guarantee required sterility levels and poses risks of infection and sepsis.

    Product
    Catalog No. 9251R1, 9251R2, 9251R3 TRACHEOSTOMY CARE SET / STERILE - LATEX FREE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0596-2024·2024-01-10

    Regard Dressing Change Kit Recalled Due to Defective Irrigation Solution

    ROi CPS LLC is recalling Regard Dressing change kits (Item 800026006) due to a defective irrigation solution component. Approximately 1,830 units distributed in Louisiana are affected.

    Product
    Regard Dressing change kit, Item Number 800026006
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0592-2024·2024-01-10

    Tracheostomy care kits recalled for sterility assurance failure

    Busse Hospital Disposables is recalling tracheostomy care kits containing Nurse Assist Sterile Normal Saline because the required sterility assurance level cannot be guaranteed. Contaminated products could cause serious infections including bloodstream, respiratory, and urinary tract infections, or sepsis.

    Product
    Catalog No. 800 TRACHEOSTOMY CARE TRAY - STERILE -LATEX FREE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0591-2024·2024-01-10

    Omnipod 5 insulin pump app bolus calculator decimal point error

    The Omnipod 5 app bolus calculator may fail to record a decimal point if entered first when adjusting a dose, potentially causing insulin over-delivery. Users should verify dose values on both the calculator and confirmation screens before administering insulin.

    Product
    Omnipod 5 App (on compatible Android smartphones), Software Versions 1.1 - 1.2.3 (current). US: PT-000599- Omnipod 5 App Software Package (provided through Google Play), EU: PT-001323- Omnipod 5 App Software Package (provided on locked-down Controllers (PT-001194 and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V013000·2024-01-10

    Western Star 4900 and 6900 Trucks Recalled for Parking Brake Defect

    Daimler Trucks North America is recalling 2023 Western Star 4900 and 6900 trucks because a parking brake defect may allow the vehicle to move unintentionally.

    Product
    WESTERN STAR — WESTERN STAR 6900, 4900
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0593-2024·2024-01-10

    Dressing change tray recalled for sterility assurance failure

    Busse Hospital Disposables recalls sterile dressing change trays due to inability to guarantee required sterility assurance level. The defect could lead to serious infections including blood stream, urinary tract, or respiratory infections.

    Product
    Catalog No. 1443 DRESSING CHANGE TRAY / STERILE - LATEX FREE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0638-2024·2024-01-10

    Philips Trilogy Evo respiratory devices recalled for missing contraindication statement

    Philips recalled Trilogy Evo respiratory devices for missing contraindications in labeling. Devices lack warnings against use in pediatric patients under 10 kg and certain therapy modes, risking barotrauma and respiratory complications.

    Product
    Trilogy Evo and Trilogy Evo O2 Material Numbers BL2110X15B BR2110X18B CA2110X12B DE2100X13B DE2110X13B DS2100X11B DS2110X11B EE2100X15B EE2110X15B ES2100X15B ES2110X15B EU2100X15B EU2100X19 EU2110X15B FR2100X14B FR2110X14B FX2100X15B GB2110X15B IA2100X15B…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0627-2024·2024-01-10

    Merit Maestro Microcatheter Sterility Recall, 717 Units Distributed Worldwide

    Merit Medical Systems is recalling 717 units of Merit Maestro Microcatheters because their sterility cannot be guaranteed. Non-sterile devices could introduce infection when used in medical procedures.

    Product
    Merit Maestro Microcatheter, Reference Numbers: 28MC2111045/B, 28MC21110ST/B, 28MC2113045/B, 28MC21130SN/CNB, 28MC21130ST/B, 28MC2115045/B, 28MC2115045/C, 28MC21150SN/B, 28MC21150ST/B, 28MC2411045/D, 28MC24110SN/D, 28MC24110ST/D, 28MC2413045/D, 28MC24130SN/F…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0664-2024·2024-01-10

    Dietary supplement recalled due to potential mold contamination

    Spring Valley Biotin & Collagen Liquid is being recalled due to potential mold contamination. Approximately 24,324 units were distributed nationwide; consumers should stop using affected products.

    Product
    Spring Valley Biotin & Collagen Liquid, Natural Berry Flavor, 15000 mcg, Dietary Supplement 29 doses 1 fl oz (29mL) UPC: 194346065158 Packaged in a glass bottle in a paper carton
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0635-2024·2024-01-10

    EDS 3 CSF External Drainage System recalled for incomplete sterility testing

    Natus Medical is recalling 3,336 units of the EDS 3 CSF External Drainage System nationwide because incomplete bioburden testing cannot guarantee sterility. No illnesses have been reported, but non-sterile devices pose infection risk.

    Product
    EDS 3 CSF External Drainage System, REF: NT821731C, STERILEEO, Rx only
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0628-2024·2024-01-10

    FDA Recalls Merit Pursue Microcatheter Due to Sterility Concerns

    Merit Medical Systems is recalling Merit Pursue Microcatheter devices distributed worldwide because sterility cannot be guaranteed. Patients should contact their healthcare provider.

    Product
    Merit Pursue Microcatheter, REF: 28HC17130SN, 28HC17150ST/A, 29HC2015045/A, 29HC20150SN/A, 29HC20150ST, CE 2797, STERILEEO, Rx ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0631-2024·2024-01-10

    Covidien Valleylab FT10 Energy Platform software issue causes inoperability

    Covidien is recalling Valleylab FT10 FT Series Energy Platform devices due to a software issue that may render new systems inoperable. The recall affects 47,901 units distributed worldwide.

    Product
    Covidien Valleylab FT10, FT Series Energy Platform, REF: VLFT10GEN, DLVLFT10GEN, VLFT10GENZD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·24V011000·2024-01-10

    2022-2023 Lucid Air defrost heater failure reduces windshield visibility

    Lucid is recalling 2022-2023 Air vehicles whose high voltage coolant heater may fail to defrost the windshield, reducing visibility and increasing crash risk. Lucid will provide a software update and replace failed heaters at no cost.

    Product
    LUCID — LUCID AIR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0218-2024·2024-01-10

    Peritoneal Dialysis Solution Recalled for Lack of Sterility Assurance

    Fresenius Medical Care is recalling 69,590 bags of DELFLEX Peritoneal Dialysis Solution due to lack of sterility assurance. The affected lot was distributed nationwide.

    Product
    DELFLEX — DELFLEX (DEXTROSE MONOHYDRATE, SODIUM CHLORIDE, SODIUM LACTATE, CALCIUM CHLORIDE, MAGNESIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·24V010000·2024-01-10

    2024 Volvo XC40 Left Rear Turn Signal May Not Function

    Certain 2024 Volvo XC40 vehicles may have a software error in the Central Electronic Module that disables the left rear turn signal indicator, increasing the risk of a crash if other drivers are not notified of turning.

    Product
    VOLVO — VOLVO XC40
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0711-2024·2024-01-10

    Racine Danish Kringles Raspberry Kringle Recalled for Undeclared Tree Nuts

    Racine Danish Kringles Raspberry Kringle (14 oz., lot 23299) is being recalled due to undeclared tree nuts (pecans). Consumers with nut allergies should not consume this product.

    Product
    Racine Danish Kringles Raspberry Kringle, 14 oz. UPC 0 45251-00312 7. RDK Corp, Racine, WI 53404.
    Category
    Food
    Distribution
    5 states