The Recall Desk

State

South Dakota product recalls

73,570 recalls have nationwide distribution and so reach South Dakota. 2,686 additional recalls listed South Dakota specifically in their distribution scope.

What the numbers show

Total
2,686
Critical
401
Severe
747
Most recent
2026-10-14

Of the 2,686 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 747 (28%) are Severe.

Which agencies issued them

These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26101–26125 of 76256

  • HighFDA (Devices)·Z-1369-2021·2021-04-14

    Hologic Recalls Panther Fusion Tube Trays Due to Potential Leakage

    Hologic is recalling 1,355 Panther Fusion Tube Trays because they may leak, potentially causing false positive, false negative, or invalid patient results.

    Product
    Panther Fusion Tube Tray, REF PRD-04000, PN: FA-15004, Cont. 18 Tube Trays - Product Usage: an ancillary consumable to the Panther Fusion System that is used to contain the PCR and RT-PCR steps of the assay processing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1348-2021·2021-04-14

    Fujifilm Synapse PACS Recalled for Potential Wrong Patient Information Display

    Fujifilm Medical Systems is recalling Synapse PACS software because it may display incorrect patient information in the viewer or PowerJacket.

    Product
    Synapse PACS - Radiological Image Processing System - Product Usage: intended for use, as a web based application, on an off-the-shelf PC meeting or exceeding minimum specifications and networked with FUJIFILM Synapse PACS Software (Server).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1368-2021·2021-04-14

    Medtronic A610 Clinician Programmer Software Recall for Deep Brain Stimulation

    Medtronic is recalling A610 Clinician Programmer software versions 2.0.4584, 2.0.4594, 2.0.4605, and 3.0.1057 due to software errors that prevent proper copying of cycling settings and cause application crashes when reading full system event logs.

    Product
    A610 Clinician Programmer Application for Deep Brain Stimulation Clinician Programming Guide Percept PC Model B35200 Neurostimulator Application, version 2.0.4584, 2.0.4594, 2.0.4605, and 3.0.1057* * Version 3.0.1057 is approved for distribution in Europe only.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1367-2021·2021-04-14

    Terumo Sternal Retractor Locking Mechanism Recall for Fracture Risk

    Terumo is recalling 12 sternal retractor devices because the stainless steel locking plates may fracture. The devices were distributed in eight US states.

    Product
    Consist of a distal connection mechanism (either standard Terumo Ball Quick Connect or Terumo Shaft Quick Connect), an articulating arm with links, a handle for providing cable tension, and a mechanism to mount the device to a sternal retractor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0327-2021·2021-04-14

    Cosette Recalls Mometasone Furoate Topical Solution Due to CGMP Deviations

    Cosette Pharmaceuticals is recalling specific lots of Mometasone Furoate Topical Solution due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    Mometasone Furoate Topical Solution, USP, 0.1%, (Lotion), a) 30 mL (NDC 0713-0701-85) and b) 60 mL (NDC 0713-0701-53), Rx Only, Distributed by: Cosette Pharmaceuticals, Inc., South Plainfield, NJ 07080
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1353-2021·2021-04-14

    Gf Health Products Recalls Drop Arm Versamode Due to Incorrect Casters

    Gf Health Products is recalling 66 units of the Drop Arm Versamode because the front casters are incorrect. The devices were distributed in the US and internationally.

    Product
    Drop Arm Versamode"
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1349-2021·2021-04-14

    Nuvasive PRECICE Limb Lengthening System Recalled for Missing Biological Assessments

    Nuvasive Specialized Orthopedics is recalling PRECICE limb lengthening devices because they lack full biological assessments and are not indicated for patients under 18.

    Product
    NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System End Cap for PRECICE Intramedullary Limb Lengthening System Implant; Packaged End Cap 8.5/10.7mm,¿ +0mm; Packaged End Cap 8.5/10.7mm,¿ +5mm; Packaged End Cap 8.5/10.7mm,¿ +10mm; Packaged End Cap…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0431-2021·2021-04-14

    Toasted Oat Macadamia Chunk Granola Recalled for Mold-Containing Ingredient

    The Toasted Oat is recalling Macadamia Chunk Soft Granola and Crumble Bars because an ingredient containing mold was used in production.

    Product
    The Toasted Oat Bakehouse Macadamia Chunk Soft Granola (6 - 10oz pouches per case); and Soft Granola Crumble Bars Macadamia Chunk ( 5 - 28.3g bars per pack/6 packs per case).
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Devices)·Z-1351-2021·2021-04-14

    Nuvasive Freedom End Caps Recalled for Missing Biological Assessments

    Nuvasive Specialized Orthopedics Inc. is recalling 59 units of Freedom End Caps and related components because they lack full biological assessments and are not indicated for patients under 18.

    Product
    NUVASIVE FREEDOM: End Cap for PRECICE Intramedullary Limb Lengthening System Implant; Packaged End Cap 8.5/10.7mm,¿ +0mm; Packaged End Cap 8.5/10.7mm,¿ +5mm; Packaged End Cap 8.5/10.7mm,¿ +10mm; Packaged End Cap 8.5/10.7mm,¿ +15mm; Packaged End Cap 8.5/10.7mm,¿ +20mm…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0433-2021·2021-04-14

    Toasted Oat Apricot Shortbread Granola Recalled for Mold Contamination

    The Toasted Oat is recalling Apricot Shortbread Soft Granola because an ingredient containing mold was used in production.

    Product
    The Toasted Oat Bakehouse Apricot Shortbread Soft Granola (6 - 10oz pouches per case)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0328-2021·2021-04-14

    X-Gen Recalls Neomycin Sulfate Tablets Due to Microbiological Failure

    X-Gen Pharmaceuticals is recalling Neomycin Sulfate Tablets 500mg because a microbiological assay failed to meet stability specifications.

    Product
    Neomycin Sulfate Tablets, USP 500mg, Rx Only, 10x10 Unit dose 100 Tablets, Manufactured for: X-GEN Phamaceuticals, Inc. Big Flats, NY 14814. NDC 39822-0310-5
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1352-2021·2021-04-14

    Clerio Vision Recalls Extreme H2O 59% Contact Lenses for Mislabeled Power

    Clerio Vision is recalling 153 Extreme H2O 59% contact lenses because they may be mislabeled with the incorrect lens power.

    Product
    EXTREME H2O 59% (hioxifilcon A) spherical soft contact lens for daily wear - Product Usage: indicated for the correction of visual acuity in aphakic or not-aphakic persons with non-diseased eyes that are myopic or hyperopic. The lens may be worn by persons who exhibit…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0430-2021·2021-04-14

    Toasted Oat Blueberry Cobbler Granola Recalled for Mold Contamination

    The Toasted Oat is recalling Blueberry Cobbler Soft Granola and Crumble Bars because an ingredient containing mold was used in production.

    Product
    The Toasted Oat Bakehouse Blueberry Cobbler Soft Granola (6 -10 oz pouches per case); and Soft Granola Crumble Bars Blueberry Cobbler (5 - 28.3g bars per pack/6 packs per case)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Food)·F-0385-2021·2021-04-14

    New Generation Wellness Recalls Vegan Vitamin D3 Tablets for Stability Issues

    New Generation Wellness Inc. is recalling 2,330 bottles of Vegan Vitamin D3 tablets because stability samples showed potency below the label claim.

    Product
    VEGAN VITAMIN D3, 50 mcg (2,000 IU), 60 VEGAN TABLETS in 100cc amber glass bottles. UPC 7 19985 61831 4; UPC 6 10265 58337 0; UPC 4 01008 61831 8; UPC 4 02008 61831 5. Store in a cool, dry place. Product is sold under 72 private labels: A Moveable Feast; Akin's Natural…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0432-2021·2021-04-14

    Toasted Oat Cherry Streusel Granola Recalled for Mold-Containing Ingredient

    The Toasted Oat is recalling Cherry Streusel Soft Granola and Crumble Bars because an ingredient containing mold was used in production.

    Product
    The Toasted Oat Bakehouse Cherry Streusel Soft Granola (6 - 10oz pouches per case); and Soft Granola Crumble Bars Cherry Streusel ( 5 - 28.3g bars per pack/6 packs per case)
    Category
    Food
    Distribution
    1 state
  • ModerateFDA (Drugs)·D-0319-2021·2021-04-14

    Kimberly-Clark Recalls Scott Moisturizing Foam Hand Sanitizer Due to Labeling Error

    Kimberly-Clark is recalling Scott Moisturizing Foam Hand Sanitizer because some bottles containing Foam Skin Cleanser soap are incorrectly labeled as hand sanitizer.

    Product
    Scott¿ Moisturizing Foam Hand Sanitizer, 1.2 Liters (40.5 fl oz), Distributed in the U.S. by Kimberly-Clark Global Sales, LLC, Roswell, GA 30076-2199 Distributed in Canada by Kimberly-Clark Inc., Mississauga, Ontario L5B 3Y5 UPC 0 36000 91592 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1350-2021·2021-04-14

    Nuvasive Precice Unyte Orthopedic Rods Recalled for Missing Biological Assessments

    Nuvasive Specialized Orthopedics is recalling Precice Unyte orthopedic trauma nails because they lack full biological assessments and are not indicated for patients under 18.

    Product
    NUVASIVE PRECICE UNYTE System (Humerus and Tibia): PRECICE Trauma Nail System/PRECICE Unyte-Humerus Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 165 mm length; Orthopedic trauma intramedullary rod, humerus, 8.5 mm diameter, 180 mm length; Orthopedic…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0325-2021·2021-04-14

    Sun Pharmaceutical Recalls Metformin Hydrochloride Extended-Release Tablets

    Sun Pharmaceutical Industries is recalling 2,520 bottles of Metformin Hydrochloride Extended-Release Tablets due to failed moisture limits.

    Product
    METFORMIN HYDROCHLORIDE — METFORMIN HYDROCHLORIDE (METFORMIN HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·F-0384-2021·2021-04-14

    CVS Live Better Vitamin D3 Recalled for Stability Issues

    New Generation Wellness Inc. is recalling Live Better vegan vitamin D-3 tablets because stability samples showed less than 100% of the label claim.

    Product
    Live Better vegan vitamin d-3 by CVS Health, 50 mcg (2000 IU), 40 tablets in blue PET jar, Distributed by: CVS Pharmacy, Inc. one CVS Drive, Woonsocket, RI 02895, UPC 0 50428 62499 9
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V258000·2021-04-13

    2021 Newmar Motorhomes Recall: Steering Column Shaft Disengagement Risk

    Newmar is recalling certain 2021 motorhomes due to a steering output shaft that may be too short and disengage from the input shaft, potentially causing loss of steering control and increased crash risk. Owners should contact Newmar for free inspection and replacement.

    Product
    NEWMAR — NEWMAR NEW AIRE, DUTCH STAR, MOUNTAIN AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V260000·2021-04-13

    Kia Recalls 2017-2018 Forte Vehicles Due to Oil Pump Defect

    Kia is recalling 2017-2018 Forte vehicles with 2.0L engines because foreign particles may cause oil pump failure and engine damage.

    Product
    KIA — KIA FORTE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V262000·2021-04-13

    Kenworth Recalls 2022 Trucks Due to Starter Interlock Defect

    PACCAR is recalling 2022 Kenworth T440, T470, T800, and W900 trucks because the starter interrupt may allow starting when the transmission is not in PARK.

    Product
    KENWORTH — KENWORTH T800B, W990, T440, T470
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V259000·2021-04-13

    2021 KIA SELTOS Engine Defect May Cause Stall or Fire

    Kia is recalling 2021 Seltos and 2020-2021 Soul vehicles due to improperly heat-treated piston rings that may cause engine damage, stalling, and crash risk, or oil leaks that may cause fires.

    Product
    KIA — KIA SOUL, SELTOS
    Category
    Vehicle
    Distribution
    Distributed nationwide