The Recall Desk

State

South Dakota product recalls

73,366 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
747
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 747 (28%) are Severe.

These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19051–19075 of 76050

  • ModerateFDA (Devices)·Z-0038-2023·2022-10-19

    Hobbs Biliary Pigtail Stent Kits recalled due to incorrect expiration date

    Hobbs Medical is recalling Biliary Pigtail Stent Kits with incorrect expiration dates on labels. The incorrect dates extend the product shelf life, potentially allowing devices to be used past their actual expiration.

    Product
    Hobbs Biliary Pigtail Stent Kits (containing 3412) Catalog Number:6004
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0068-2023·2022-10-19

    Hobbs Medical Polypectomy Snare Recalled for Incorrect Expiration Dates

    Hobbs Medical is recalling polypectomy snares with incorrect expiration dates on labels. Affected devices have lot numbers ending in R and were distributed from March 2018 to September 2020.

    Product
    Hobbs Medical Polypectomy Snare Catalog Number: 4563-OLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0029-2023·2022-10-19

    Hobbs Helical Retrieval Basket Recall: Incorrect Device Label Expiration Date

    Hobbs Medical is recalling Helical Retrieval Baskets due to incorrect expiration dates on device labels. The mislabeling extends the shelf life, potentially allowing use of expired devices.

    Product
    Hobbs Helical Retrieval Basket Catalog Number: 4816
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0083-2023·2022-10-19

    Prismaflex HF medical device sets recalled for instructional mistranslation

    Baxter Healthcare recalls Prismaflex HF Set devices due to a mistranslation in Estonian language instructions. The mistranslation contains contradictory information about patient body weight restrictions.

    Product
    Prismaflex HF Set: HF1000 (product code 107140), HF1400 (product code 107142). For use in providing continuous fluid management and renal replacement therapies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0014-2023·2022-10-19

    Hobbs Medical Cytology Brush Recalled for Incorrect Expiration Date Labeling

    Hobbs Medical is recalling Cytology Brush Catalog Number 4206 due to incorrect expiration dates on product labels that extend the intended shelf life. Approximately 300 units were distributed nationwide and internationally between March 2018 and September 2020.

    Product
    Hobbs Medical Cytology Brush Catalog Number: 4206
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0048-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Kit recalled for mislabeled expiration dates

    Hobbs Medical is recalling the Freeman Pancreatic Flexi-Stent Kit because the device label displays an incorrect expiration date that extends the shelf life. U.S. distribution of affected devices occurred between March 25, 2018 and September 28, 2020.

    Product
    Freeman Pancreatic Flexi-Stent Kit Catalog Number: 6352
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0033-2023·2022-10-19

    Hobbs Helical Retrieval Basket Recalled for Incorrect Expiration Date

    Hobbs Medical, Inc. is recalling Hobbs Helical Retrieval Baskets with lot numbers ending in R due to incorrect expiration dates on device labels. Affected units were distributed worldwide from March 2018 to September 2020.

    Product
    Hobbs Helical Retrieval Basket Catalog Number: 4832
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0080-2023·2022-10-19

    Clip COVID Rapid Antigen Test Kit Recalled for Unapproved Shelf-Life Extension

    LUMINOSTICS recalled Clip COVID test kits because the manufacturer extended shelf life and expiration dates without FDA approval. The extended expiration dates lack FDA validation.

    Product
    Clip COVID Rapid Antigen Test Kit (25-pack), Catalog Number: MDL002
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0057-2023·2022-10-19

    Freeman Pancreatic Flexi-Stent Recall Due to Incorrect Expiration Date Label

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices with incorrect expiration dates on labels. Affected units distributed in the US and internationally from 2018 to 2020 may have extended shelf lives beyond accuracy.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6535
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0011-2023·2022-10-19

    Hobbs Medical Spray Catheter Recalled for Incorrect Expiration Date on Label

    Hobbs Medical Spray Catheter devices sold between March 2018 and September 2020 have incorrect expiration dates on their labels. The error may extend the device's shelf life beyond its actual expiration.

    Product
    Hobbs Medical Spray Catheter: The Mistifier: 2.6mm 165cm Disposable For endoscopy procedures Ref: 2191
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0063-2023·2022-10-19

    Pancreatic stent recall due to incorrect expiration date on device labels

    Hobbs Medical is recalling Freeman Pancreatic Flexi-Stent devices distributed between March 2018 and September 2020 due to incorrect expiration dates on product labels. The mislabeled devices display extended shelf-life information that does not reflect actual product safety.

    Product
    Freeman Pancreatic Flexi-Stent Catalog Number: 6568
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0085-2023·2022-10-19

    Prismaflex HF20 Medical Device Recall Due to Mistranslated Instructions

    Baxter Healthcare recalls the Prismaflex HF20 Set due to a mistranslation in device instructions that creates contradictory information about patient weight restrictions. The issue affects 29,764 devices distributed nationwide.

    Product
    Prismaflex HF20 Set (product code 109841). For use in providing continuous fluid management and renal replacement therapies.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V782000·2022-10-18

    PACCAR Recalls 2023 Kenworth and Peterbilt Trucks for Steering Defect

    PACCAR is recalling 2023 Kenworth and Peterbilt trucks because improperly heat-treated tie rod clamps may fail, causing a sudden loss of steering.

    Product
    KENWORTH — KENWORTH, PETERBILT T800B, W900, T370, T480
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E089000·2022-10-18

    Comoto Recalls Youth Helmets for Inadequate Impact Protection

    Comoto is recalling specific Bilt Grommet Youth helmets that may not adequately protect the wearer during a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V781000·2022-10-18

    Harley-Davidson Touring and Trike Motorcycles Unintended Brake Light Illumination Recall

    Harley-Davidson is recalling certain 2019-2022 Touring, Trike, and CVO models due to a software error causing brake lights to illuminate without rider input. This malfunction may confuse other drivers and increase crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLTRXS, FLTRXSE, FLTRXST, FLHTCUTGSE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V778000·2022-10-17

    Spartan Fire Recalls Emergency Vehicles Due to Tie Rod Clamp Defect

    Spartan Fire is recalling 2021-2023 emergency vehicles because improperly heat-treated tie rod clamps may fail, causing loss of steering.

    Product
    SPARTAN FIRE — SPARTAN FIRE, KME METROSTAR, GLADIATOR, FC-94, redundant PANTHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V779000·2022-10-17

    Peterbilt and Kenworth trucks recalled for digital display freeze

    PACCAR is recalling certain 2022-2023 Kenworth and Peterbilt trucks whose digital displays may freeze. A frozen display prevents critical safety information like vehicle speed and warning lights from appearing.

    Product
    KENWORTH — KENWORTH, PETERBILT T680, 579, 367, T880
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V777000·2022-10-14

    HD Trailer Recalls 2022 Non-CDL Goosenecks Due to Axle Weld Defect

    HD Trailer is recalling 2022 Non-CDL Gooseneck trailers because improper axle spindle welds may crack or separate, increasing crash risk.

    Product
    HD TRAILER — HD TRAILER NON CDL GOOSENECKS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V773000·2022-10-14

    Jayco Recalls 2021-2022 Travel Trailers Due to Cooktop Flame Inversion Risk

    Jayco is recalling 2021-2022 Jay Feather, Jay Flight, and Jay Flight SLX travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire and injury risks.

    Product
    JAYCO TRAVEL TRAILER — JAYCO TRAVEL TRAILER JAY FLIGHT SLX, JAY FLIGHT, JAY FEATHER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V775000·2022-10-14

    Highland Ridge Travel Trailers Recalled for Cooktop Flame Inversion Risk

    Highland Ridge RV is recalling 2021-2022 travel trailers because the cooktop flame may invert when the stove and furnace operate simultaneously, increasing fire and injury risks.

    Product
    HIGHLAND RIDGE TT — HIGHLAND RIDGE TT OPEN RANGE LIGHT, OPEN RANGE, OLYMPIA SPORT, OLYMPIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V771000·2022-10-13

    GM Recalls 2022-2023 Hummer EV and BrightDrop EV600 for Battery Seal Defect

    General Motors is recalling 2022-2023 Hummer EV Pickups and 2022 BrightDrop EV600s because the high-voltage battery pack may not be sealed, allowing water entry that can cause loss of drive power.

    Product
    BRIGHTDROP — BRIGHTDROP, GMC EV600, HUMMER EV PICKUP
    Category
    Vehicle
    Distribution
    Distributed nationwide