The Recall Desk

State

South Dakota product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25501–25525 of 76252

  • SevereFDA (Food)·F-0624-2021·2021-06-02

    American Pop Corn Recalls Buttered Microwave Popcorn for Undeclared Milk Allergen

    American Pop Corn Co. is recalling buttered microwave popcorn bags packaged in boxes that fail to declare the major food allergen milk.

    Product
    Xtra Butter Microwave Popcorn bags packaged in cardboard boxes labeled to be Jolly Time Healthy Pop 100's Kettle Corn 100 Calorie Singles, 3 1.2 oz (34 g) Net Wt 4.8 oz (136 g), American Pop Corn Co. Sioux City, Iowa
    Category
    Food
    Distribution
    16 states
  • SevereFDA (Devices)·Z-1630-2021·2021-06-02

    Philips Respironics BiPAP A40 Ventilator Recall for Material Defects

    Philips Respironics is recalling four BiPAP A40 ventilators because non-conforming plastic in the motor assembly may cause toxic off-gassing or sudden device failure.

    Product
    BiPAP A40, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111169
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1626-2021·2021-06-02

    Philips Respironics BiPAP A40 Ventilators Recalled for Motor Assembly Defects

    Philips Respironics is recalling 10 BiPAP A40 ventilators due to non-conforming plastic in motor assemblies that may cause toxic off-gassing or sudden device failure.

    Product
    BiPAP A40, China: Continuous ventilator, non-life-supporting. Material Number - CN1111169
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1627-2021·2021-06-02

    Philips BiPAP A40 System Silver Recalled for Motor Assembly Defects

    Philips Respironics is recalling specific BiPAP A40 System Silver units due to non-conforming plastic in motor assemblies that may cause off-gassing or sudden device failure.

    Product
    BiPAP A40 System Silver, JP: Continuous ventilator, non-life-supporting. Material Number: R1111177
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0632-2021·2021-06-02

    Sara Lee and Chef Pierre Pecan Pies Recalled for Undeclared Peanut

    Sara Lee Frozen Foods is recalling specific pecan pie products due to potentially undeclared peanut. Consumers should check labels and stop using the affected items.

    Product
    Sara Lee Pecan Pie 4oz. retail packaged UPC 032100051118, 24 and 48 count wholesale case; Chef Pierre Southern Pecan Pie, 10 slices, 36oz. retail packaged UPC 032100092739, 6 pies per wholesale case; Chef Pierre Pecan Pie, 10 slices, 36oz. retail packaged UPC 032100093750, 6…
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1629-2021·2021-06-02

    Philips Respironics BiPAP A30 Ventilator Recall for Motor Assembly Defect

    Philips Respironics is recalling two BiPAP A30 ventilators due to non-conforming plastic in motor assemblies that may cause toxic off-gassing or sudden device failure.

    Product
    BiPAP A30, Brazil: Continuous ventilator, non-life-supporting. Material Number: BR1111143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V414000·2021-06-02

    Volvo Recalls 2019-2020 Models for Fuel Pump Fuse Failure Risk

    Volvo is recalling 2019-2020 models because a fuel pump fuse can fail, causing the vehicle to stall and increasing crash risk.

    Product
    VOLVO — VOLVO V60CC, V90CC, V90, XC60
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0399-2021·2021-06-02

    Acella Recalls Subpotent NP Thyroid 15 Tablets Nationwide

    Acella Pharmaceuticals is recalling NP Thyroid 15 tablets because they contain less active ingredient than labeled. The recall covers bottles distributed nationwide.

    Product
    NP THYROID 15 — NP THYROID 15 (LEVOTHYROXINE, LIOTHYRONINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V418000·2021-06-02

    Stonebrooke RAM 5500 Recalled for Rear Brake Fluid Leak Risk

    Stonebrooke is recalling one 2019 RAM 5500 because the rear brake line can wear and leak, increasing crash risk.

    Product
    STONEBROOKE EQUIPMENT — STONEBROOKE EQUIPMENT RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0561-2021·2021-06-02

    Wild Rice Split Pea Soup Recalled for Undeclared Wheat and Soy

    The Secret Garden of Park Rapids is recalling Wild Rice Split Pea Soup because it contains undeclared wheat and soy allergens.

    Product
    Wild Rice Split Pea Soup, UPC 91675-71000, The Secret Garden, Park Rapids, MN 56470
    Category
    Food
    Distribution
    4 states
  • HighFDA (Food)·F-0626-2021·2021-06-02

    Brill Inc Recalls Chocolate Chip Cookies for Potential Foreign Objects

    Brill Inc is recalling specific batches of 12-inch chocolate chip message cookies due to a potential risk of containing small foreign objects.

    Product
    10194739 TranSmart" 12 INCH CHOCOLATE CHIP MESSAGE COOKIE 24/24 OUNCE CHOCOLATE CHIP COOKIES IN BAKEABLE PLASTIC PANS WITH DOMES KEEP FROZEN AT 0¿F OR BELOW Net weight: 36 lb (16.33 kg) (24 x 24 oz (680g))
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·21V415000·2021-06-02

    Genesis Supreme Wanderer and Vortex RV Trailers Recalled for Cooking Stove Gas Leak

    Genesis Supreme RV is recalling certain 2020-2021 Wanderer and Vortex trailers with Dometic cooking stoves. An overtightened saddle valve securing bolt can damage the seal and cause a gas leak, increasing fire risk.

    Product
    GENESIS SUPREME — GENESIS SUPREME VORTEX, WANDERER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21E049000·2021-06-02

    Adventurer Truck Campers Recalled for Potential Gas Leak from Dometic Stoves

    Adventurer LP is recalling specific truck campers equipped with Dometic stoves because a saddle valve bolt may be overtightened, causing a gas leak that increases fire risk.

    Product
    EQUIPMENT:APPLIANCE:OVEN/STOVE/COOKTOP recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1683-2021·2021-06-02

    Radiometer Recalls PICO70 Arterial Blood Samplers Due to Sterile Barrier Breach

    Radiometer is recalling PICO70 Arterial Blood Samplers because a sterile barrier breach was found during testing, posing a risk of bacterial infection.

    Product
    PIC070 Arterial Blood Sampler PICO70 - Product Usage: Preheparinized, electrolyte-balanced, arterial blood sampler product line for collection of arterial samples for pH, blood gas, oximetry, electrolyte and metabolite analysis. Model Number/Product Description: 956-518…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1672-2021·2021-06-02

    Welch Allyn GS777 Wall Transformer Recalled for Electrical Shock Risk

    Welch Allyn is recalling GS777 Wall Transformers due to a potential risk of fluid ingress causing electrical shorts and shock.

    Product
    GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall Transformer is intended for use in ambulatory and acute care settings.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V413000·2021-06-02

    2021 Volkswagen ID.4 recalled for incorrect headlight aiming caps

    Volkswagen is recalling certain 2021 ID.4 vehicles because headlight aiming caps were installed on the vertical adjustment instead of the horizontal adjustment. This defect can increase glare and reduce visibility, increasing the risk of a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ID.4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0627-2021·2021-06-02

    Brill Inc Recalls Jumbo Chocolate Chip Cookies Due to Foreign Objects

    Brill Inc is recalling Jumbo Chocolate Chip Cookies nationwide because they may contain small foreign objects.

    Product
    10233579 JUMBO CHOCOLATE CHIP COOKIE 12 / 12 INCH BAKED CHOCOLATE CHIP COOKIES KEEP FROZEN Net weight: 17.04 lb (7.73 kg)
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1670-2021·2021-06-02

    Beckman Coulter Access SARS-CoV-2 Antigen Recalled for False Negative Risk

    Beckman Coulter is recalling Access SARS-CoV-2 Antigen test kits because specimens stored in certain conditions may yield false negative results.

    Product
    Access SARS-CoV-2 Antigen, REF C68668, UDI: (01)15099590742713, 3.30 mL/R1a, 4.70 mL/R1b, 4.20 mL/R1c, 3.10 mL, R1d, 3.10 mL, R1e
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·21V416000·2021-06-02

    Mack 2021-2022 trucks recalled for hubcap separation hazard

    Mack Trucks is recalling 307 certain 2021-2022 Granite, Pinnacle, and Anthem commercial trucks due to a defective hubcap compression spring that can cause the hubcap to separate, creating a road hazard and increasing crash risk.

    Product
    MACK — MACK ANTHEM (AN), GRANITE (GR), PINNACLE (CHU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V410000·2021-06-02

    Mercedes-Benz Sprinter Recall for Swivel Seat Wiring Harness Defect

    Daimler Vans USA is recalling 2019-2021 Mercedes-Benz and Freightliner Sprinter vans with swivel seats because incorrect wiring harness routing may damage the seat air bag system.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1682-2021·2021-06-02

    Pentax Medical Video Duodenoscope Recalled for Distal End Cap Detachment Risk

    Pentax of America Inc. is recalling 108 Pentax Medical Video Duodenoscopes because the distal end cap may detach during procedures, posing risks of injury or aspiration.

    Product
    Pentax Medical Video Duodenoscope - Product Usage: intended to be used with endoscopic devices and other ancillary equipment to provide optical visualization of (via a video monitor), and therapeutic access to, Biliary Tract via the Upper Gastrointestinal Tract, Model Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1673-2021·2021-06-02

    Welch Allyn ProBP 3400 Digital Blood Pressure Device Recall

    Welch Allyn is recalling ProBP 3400 Digital Blood Pressure Devices due to a risk of fluid ingress causing electrical shorts and potential shock.

    Product
    ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount models) Model: 34XFHT-B Intended: ProBP 3400 automatically measures systolic and diastolic pressure (excluding neonates) and pulse rate, as well as calculates Mean Arterial Pressure (MAP).
    Category
    Medical Device
    Distribution
    Distributed nationwide