The Recall Desk

State

South Dakota product recalls

73,190 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.

Which agencies issued them

These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,190 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

14476–14500 of 75874

  • ModerateFDA (Drugs)·D-0039-2024·2023-10-11

    HydrALAZINE Hydrochloride Tablets recalled due to impurity specifications failure

    Amerisource Health Services LLC is recalling HydrALAZINE Hydrochloride Tablets, 10 mg, nationwide due to impurities exceeding specifications in a repackaged product batch.

    Product
    HydrALAZINE Hydrochloride Tablets, USP, 10 mg, 100 Tablets (10 x 10) per carton, Rx Only, Distributed by: American Health Packaging, Columbus, Ohio 43217. Carton NDC#: 68084-447-01; Individual Dose NDC: 68084-447-11
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0034-2024·2023-10-11

    Dr. Berne's MSM MIST 15% Topical Spray Recalled for Manufacturing Deviations

    Dr. Berne's Whole Health Products has voluntarily recalled Dr. Berne's MSM MIST 15% Solution (30 mL bottles) due to Current Good Manufacturing Practice (CGMP) deviations identified during manufacturing. The recall affects 795 bottles distributed nationwide and internationally.

    Product
    Dr. Berne's MSM MIST 15% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, [email protected].
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0036-2024·2023-10-11

    Drug Recall: Dr. Berne's MSM Drops for Manufacturing Practice Violations

    Dr. Berne's MSM DROPS 5% Solution is being recalled due to Current Good Manufacturing Practice (CGMP) deviations. The voluntary recall affects 3833 bottles distributed nationwide and internationally.

    Product
    Dr. Berne's MSM DROPS 5% Solution, 30 mL/1.014 OZ bottle, Distributed by: Dr. Berne's Whole Health Products, Tesuque, NM, 87574, [email protected], UPC 00854582001111.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0038-2024·2023-10-11

    Oxybutynin Extended-Release Tablets Recalled for Failed Dissolution Specifications

    Zydus Pharmaceuticals recalls Oxybutynin Chloride Extended-Release Tablets 10 mg nationwide because the medication failed dissolution specifications. Affected lot numbers: M300652 and M300651.

    Product
    OXYBUTYNIN — OXYBUTYNIN (OXYBUTYNIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2648-2023·2023-10-11

    Siemens MAGNETOM headphones may create artifacts during MRI imaging

    Siemens Medical Solutions is recalling over-ear headphones used with MAGNETOM MRI systems. Lubricating grease in the headband may cause visible imaging artifacts during head examinations.

    Product
    (1) Over-ear headphones used with the MAGNETOM Amira MAGNETOM Free.Star MAGNETOM Sempra, MAGNETOM Free.Max, MAGNETOM Mica MAGNETOM Spectra Siemens Model Number:11060845 Used with the following MAGNETOM MRI Systems: MAGENTOM Amira 10836777 & 10838610; MAGENTOM Free.Max…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2657-2023·2023-10-11

    Medtronic Restore Clinician Programmer software recalled for compatibility issue

    Medtronic is recalling Restore Clinician Programmer Application Software due to compatibility issues with legacy software that prevent communication with implanted neurostimulators. The recall affects 2,408 devices worldwide.

    Product
    Restore Clinician Programmer Application Software, model number A71100, used with the Restore Neurostimulators.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V678000·2023-10-09

    Lightning eMotors Recalls FT3 Vehicles for Instrument Cluster Warning Light Defect

    Lightning eMotors is recalling 239 FT3-40, FT3-80, and FT3-120 vehicles because the instrument cluster may fail to activate brake, park, and ABS warning lights during startup.

    Product
    LIGHTNING EMOTORS — LIGHTNING EMOTORS FT3-40, FT3-80, FT3-120
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V676000·2023-10-06

    Mercedes-Benz Recalls 2022-2023 AMG SL55 and SL63 for Wiring Defect

    Mercedes-Benz is recalling 2022-2023 AMG SL55 and SL63 vehicles because an improperly secured electrical wiring harness may overheat or cause a short circuit, increasing the risk of fire or loss of drive power.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG SL55, AMG SL63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V675000·2023-10-06

    2020-2022 Ford Explorer Driveshaft Disconnection Risk

    Ford is recalling certain 2020-2022 Explorer vehicles because the rear axle mounting bolt may fracture, causing the driveshaft to disconnect. This can result in loss of drive power or vehicle rollaway, increasing crash risk.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V677000·2023-10-06

    Mercedes-Benz Recalls One 2022 EQB 350 for Child Seat Anchor Covers

    Mercedes-Benz is recalling one 2022 EQB 350 vehicle because incorrect child seat anchor covers may have been installed, potentially leading to improper child restraint installation.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQB 350 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalCPSC·24002·2023-10-05

    Cocco Candy Rolling Candy Recalled Due to Choking Hazard

    KGR Distribution Corp. recalls Cocco Candy Rolling Candy in multiple flavors because the candy's rolling ball can dislodge and pose a choking hazard. One death has been reported.

    Product
    Cocco Candy Rolling Candy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24701·2023-10-05

    Capri Blue Pet Products Recalled Due to Bacterial Contamination Risk

    CURiO Brands is recalling approximately 59,000 Capri Blue pet sprays and shampoos distributed from June through August 2023 because they can contain Pseudomonas aeruginosa bacteria, which poses a risk of serious infection to people with weakened immune systems or external medical devices.

    Product
    Capri Blue Pet Sprays and Shampoos
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·23V673000·2023-10-05

    Jayco Precept and Entegra Coach motorhomes: window shade emergency exit obstruction

    Jayco is recalling 2024 Precept and Entegra Coach Vision XL motorhomes because their window shades may obstruct emergency exit windows. Obstructed emergency exits could delay occupant evacuation during emergencies.

    Product
    ENTEGRA — ENTEGRA, JAYCO VISION XL, PRECEPT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24001·2023-10-05

    Candy Dynamics Recalls Slime Licker Sour Rolling Liquid Candy for Choking Hazard

    Candy Dynamics is recalling approximately 70 million Slime Licker Sour Rolling Liquid Candies because the rolling ball can detach from the container, posing a choking hazard to children. Two reports of ball detachment have been received with no injuries reported.

    Product
    Slime Licker Sour Rolling Liquid Candy
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24004·2023-10-05

    Children's Blanket Sleepers and Robes Recalled for Burn Hazard

    International Intimates is recalling Rene Rofe Girl Children's Blanket Sleepers and Hooded Robes because they fail to meet federal flammability standards for children's sleepwear, posing a burn injury risk to children ages 6–14.

    Product
    Rene Rofe Girl Children's Blanket Sleepers and Hooded Robes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24003·2023-10-05

    Russound MCA-88 Multizone Controller Amplifiers Recalled for Fire Hazard

    Russound is recalling about 3,170 MCA-88 Multizone Controller Amplifiers because internal circuit board components can overheat and catch fire. The firm has received 16 reports of smoking, charring, and burning, though no injuries have been reported.

    Product
    Russound MCA-88 Multizone Controller Amplifiers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V671000·2023-10-04

    Volkswagen Recalls 2019 Atlas Vehicles Due to Driver Side Air Bag Defect

    Volkswagen is recalling 2019 Atlas vehicles because the driver's side air bag may be missing a weld, which could cause it to deploy improperly or detach in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23E075000·2023-10-04

    Dorman Recalls Front Suspension Ball Joints Due to Steering Loss Risk

    Dorman Products is recalling specific front suspension ball joints because the ball stud may separate, leading to loss of steering control and increased crash risk.

    Product
    SUSPENSION:FRONT:CONTROL ARM:LOWER BALL JOINT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2644-2023·2023-10-04

    B.Braun NORM-JECT Luer Lock Solo 10ml Syringe Sterility Recall

    B.Braun NORM-JECT Luer Lock Solo 10ml sterile syringes are being recalled because the sterile blister packaging may be damaged, potentially compromising sterility. The recall affects 604,800 units distributed nationwide.

    Product
    B.Braun NORM-JECT Luer Lock Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. Distributed by: Air-Tite Products Co., Inc, 565 Central Drive, Virginia Beach, VA 23454. REF: NJ-4606728-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2643-2023·2023-10-04

    B. Braun NORM-JECT Sterile Syringes Recalled Due to Packaging Damage

    B. Braun NORM-JECT Luer Solo 10 ml sterile syringes are recalled because blister packaging may be damaged, potentially compromising sterility. Approximately 534,000 units are affected; lot numbers 22M28C8 and 23A09C8 are included.

    Product
    B. Braun NORM-JECT Luer Solo, 10 ml, Sterile-Intended to be used to deliver (inject) or withdraw an accurate metered dose of a fluid to/from the body. Distributed by: Air-Tite Products Co., Inc, 565 Central Drive, Virginia Beach, VA 23454. REF: NJ-4606108-02
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2640-2023·2023-10-04

    3M Attest Biological Indicators Cap May Melt During Sterilization

    3M is recalling 77,280 Attest biological indicators due to caps that may melt, deform, or crack during steam sterilization cycles, potentially compromising process validation.

    Product
    3M Attest Super Rapid 5 Steam-Plus Steam Challenge Pack, REF 41482VF; designed to qualify and monitor dynamic-air removal steam sterilization processes
    Category
    Medical Device
    Distribution
    Distributed nationwide