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.

Which agencies issued them

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.

19101–19125 of 76050

HighFDA (Devices)·Z-0003-2023·2022-10-12
Handheld UV-C Germicidal Wand Recalled for Excessive Radiation Exposure
IN MY BATHROOM LLC is recalling 485 units of the Seago SG-153 handheld UV-C germicidal wand nationwide due to excessive ultraviolet-C radiation. Consumers should stop using the device and contact the manufacturer for instructions.
Product
The product is a handheld ultraviolet-C germicidal wand and contains two, narrow-diameter, tubular lamps with a peak emission wavelength in the 254 nm range.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0007-2023·2022-10-12
Zimmer G7 Acetabular System shells recalled due to packaging defect
Zimmer, Inc. is recalling certain G7 Acetabular System acetabular shells (52 MM and 60 MM) because the outer sterile package has corner walls thinner than specification, which could crack during transit and potentially lead to surgical complications or infection.
Product
G7 Acetabular System, Acetabular Shell, Item numbers Item Numbers: 010000663 (52 MM E), 010000667 (60 MM G). used in hip arthroplasty
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0006-2023·2022-10-12
Orthopedic implant recall due to labeling mismatch on Stryker EVOLVE Proline Stem
Wright Medical Technology recalls 32 units of Stryker EVOLVE Proline Stem due to labeling mismatch: outer packages are labeled with one stem size but contain a different size. Surgeons should verify device size before implantation.
Product
stryker EVOLVE, Proline Stem, CoCr, Size: +4, OD: 9.5mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V763000·2022-10-12
Blue Bird Recalls 2023 Transit Buses for Non-Compliant Door Handrails
Blue Bird is recalling 2023 Vision and All-American transit buses because the entrance door handrail diameter is too small to meet ADA standards, posing a slip and fall risk.
Product
BLUE BIRD — BLUE BIRD ALL AMERICAN TRANSIT BUS, VISION TRANSIT BUS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0005-2023·2022-10-12
Wright Medical EVOLVE Proline Stem Labeling Error Recall
Wright Medical is recalling EVOLVE Proline Stem devices due to labeling errors where the outer package does not match the device inside. Affected devices are size-mismatched, which could lead to incorrect surgical placement.
Product
stryker EVOLVE, Proline Stem, CoCr, Size: +2, O: 705mm, REF 496S275, Wright s EVOLVE Proline Plus Radial Head and Repair System is a set configuration designed to address radial head fractures. It combines parts of two systems: EVOLVE Proline and EVOLVE TRIAD.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1858-2022·2022-10-12
Hologic BioZorb LP Implant Markers Recalled Due to Mislabeled Expiration Date
Hologic recalls 233 BioZorb LP Markers nationwide due to removable labels showing incorrect expiration dates. Implants labeled with January 2022 dates may be mistakenly used after their actual July 2024 expiration.
Product
The BioZorb LP Marker is an implantable radiopaque marker used to facilitate visualization of a soft tissue site. The BioZorb LP Marker is comprised of a bioabsorbable PLA (polylactic acid) component which resorbs completely in 1 year or more and a permanent component…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0008-2023·2022-10-12
Hammertoe Continuous Compression Implant Kit Drill Pin Incompatibility
Synthes is recalling Hammertoe Continuous Compression Implant (CCI) Kits because the drill pin is incompatible with the included drill template, which may delay surgery or cause soft tissue damage and adverse tissue reactions.
Product
Hammertoe Continuous Compression Implant (CCI) Kit Part Number: 46.239.001
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·22V764000·2022-10-12
2022 Volkswagen ID.4 Rearview Camera May Be Delayed or Deactivated
2022 Volkswagen ID.4 vehicles have rearview cameras that may be delayed or deactivated, reducing rear visibility and increasing the risk of crashes. Dealers will provide a free software update.
Product
VOLKSWAGEN — VOLKSWAGEN ID.4
Category
Vehicle
Distribution
Distributed nationwide
ModerateFDA (Food)·F-0030-2023·2022-10-12
Herbal Dietary Supplement Recalled for High Bacterial Growth
Eden's Answers Inc is recalling Sprigs Dental Health, an herbal dietary supplement, due to detection of high bacterial growth. The product was distributed across 37 states.
Product
Sprigs - Dental Health: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case
Category
Food
Distribution
37 states
ModerateFDA (Food)·F-0031-2023·2022-10-12
Herbal Dietary Supplement Sprigs Honey Herbal Syrup Recalled for Bacterial Growth
Eden's Answers Inc is recalling Sprigs Honey Herbal Syrup dietary supplement due to high bacterial growth within the product. The affected product was distributed across multiple states.
Product
Sprigs - Honey Herbal Syrup: Herbal Dietary Supplement 8oz glass amber bottles with black dropper, 12 units per case
Category
Food
Distribution
37 states
ModerateFDA (Drugs)·D-0007-2023·2022-10-12
Phytonadione Injectable Emulsion recalled for failed stability testing
Dr. Reddy's Laboratories is recalling Phytonadione Injectable Emulsion USP due to out-of-specification aluminum content results found during 12-month stability testing.
Product
PHYTONADIONE — PHYTONADIONE (PHYTONADIONE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-1551-2022·2022-10-12
Tranexamic Acid Injection Recalled for Metal Particulate Matter
AuroMedics Pharma LLC is recalling one lot of Tranexamic Acid Injection due to the presence of metal particles found in a vial. The affected product was distributed nationwide.
Product
TRANEXAMIC ACID — TRANEXAMIC ACID (TRANEXAMIC ACID)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V759000·2022-10-11
FCA Recalls 2019-2020 Ram 4500 and 5500 for Brake Hose Defect
FCA US is recalling 2019-2020 Ram 4500 and 5500 Cab Chassis vehicles because rear brake hoses may rupture, causing loss of braking ability.
Product
RAM — RAM 4500, 5500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V760000·2022-10-11
Kia K5 Transmission Malfunction May Cause Complete Loss of Drive Power
Kia is recalling certain 2021-2023 K5 and 2021-2022 Sorento vehicles with transmission oil pump malfunction that may cause complete loss of drive power, increasing crash risk.
Product
KIA — KIA K5, SORENTO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V761000·2022-10-11
Alamo Recalls 2021-2022 Schwarze A9SE Monsoon Street Sweepers
Alamo Group is recalling 2021-2022 Schwarze A9SE Monsoon street sweepers because the hydraulic lift system may continue rising after disengagement, posing an injury risk.
Product
SCHWARZE — SCHWARZE A9SE MONSOON
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22E086000·2022-10-11
Chrysler Recalls Mopar Brake Hoses Due to Rupture Risk
Chrysler is recalling specific Mopar brake hoses because the inside diameter may be too small, causing rupture and loss of braking ability.
Product
SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:HOSES, LINES/PIPING, AND FITTINGS recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V758000·2022-10-10
Wabash National Recalls 2020-2023 RFALHSA Trailers for Visibility Defect
Wabash National is recalling 2020-2023 RFALHSA trailers because the lift gate obscures rear conspicuity tape, reducing visibility and increasing crash risk.
Product
WABASH NATIONAL — WABASH NATIONAL RFALHSA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V757000·2022-10-10
Fontaine Recalls 2020-2023 Elgin Sweepers Due to Air Line Defect
Fontaine is recalling 56 Elgin sweepers because a braided air line may rub through an oil tube, causing pump failure and loss of power.
Product
ELGIN SWEEPER — ELGIN SWEEPER CROSSWIND 1 (PB 220)
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V756000·2022-10-09
KZRV Recalls 2023 Durango Travel Trailers Due to Missing Emergency Exit
KZRV is recalling 2023 Durango travel trailers because the living room slide-out window may lack an emergency exit, potentially delaying evacuation during an emergency.
Product
KZRV — KZRV DURANGO
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V755000·2022-10-08
Riverside Recalls 2023 Travel Trailers Due to Awning Seam Defect
Riverside RV is recalling 2023 Retro, Intrepid, and Xplorer travel trailers because a welded seam on the electric awning may separate, posing an injury risk.
Product
RIVERSIDE — RIVERSIDE XPLORER, INTREPID, RETRO
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V753000·2022-10-07
Volkswagen Atlas Engine Bearing Defect Recall 2022 through 2023
Volkswagen is recalling 2022 and 2023 Atlas and Cross Sport vehicles because engine connecting rod bearings may become damaged, causing engine failure and stalling. This increases crash and fire risk.
Product
AUDI — AUDI, VOLKSWAGEN Q5 SPORTBACK, Q5, ATLAS CROSS SPORT, ATLAS
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V748000·2022-10-07
2023 Newmar Dutch Star Motorhome Brake Pedal Contact May Cause Brake Failure
Newmar is recalling certain 2023 Dutch Star motorhomes because the brake pedal may contact the dash panel, causing unintended brake engagement. This can lead to brake failure and increase crash risk.
Product
NEWMAR — NEWMAR DUTCH STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·22V754000·2022-10-07
Shyft Group Recalls 2022 Utilimaster Walk-In Vans for Transmission Cable Fire Risk
Shyft Group is recalling 451 2022 Utilimaster Walk-In vans because the transmission shifter cable may contact the exhaust manifold, posing fire and crash risks.
Product
UTILIMASTER — UTILIMASTER WALK-IN VAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V752000·2022-10-07
2022 BMW motorcycles recalled for improperly lubricated clutch cover bolts
BMW is recalling certain 2022 and 2023 motorcycles with improperly lubricated clutch cover bolts that may loosen and cause oil leaks, increasing crash and fire risks. Free bolt replacement is available through BMW dealers.
Product
BMW — BMW S 1000 R, S 1000 XR, M 1000 RR, S 1000 RR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V749000·2022-10-07
Newmar Recalls 2020-2023 Super Star Motorhomes for Incorrect Tire Labeling
Newmar is recalling 2020-2023 Super Star motorhomes because the Federal Certification label may list incorrect rear tire sizes, potentially leading to improper tire installation.
Product
NEWMAR — NEWMAR SUPER STAR
Category
Vehicle
Distribution
Distributed nationwide