State

South Dakota product recalls

73,584 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: 399
Severe: 749
Most recent: 2026-10-14

Of the 2,686 recalls naming South Dakota we have scored against our rubric, 399 (15%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 749 (28%) are Severe.

Which agencies issued them

These figures cover only the 2,686 recalls whose distribution notice names South Dakota specifically. The 73,584 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

27501–27525 of 76270

ModerateFDA (Devices)·Z-0521-2021·2020-12-09
Chromsystems Saliva Calibrator Set Recalled for Stability Issues
Chromsystems is recalling 6PLUS1 Multilevel Saliva Calibrator Sets because they may not meet stability criteria, potentially causing increased cortisone results in patient samples.
Product
6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva, Order No. 73039 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0523-2021·2020-12-09
Chromsystems Recalls MassChrom Cortisol and Cortisone Saliva Control Level II Kits
Chromsystems is recalling MassChrom Cortisol, Cortisone Saliva Control Level II kits because control lots may not meet stability criteria, potentially causing increased results for patient cortisone samples.
Product
MassChrom Cortisol, Cortisone Saliva Control Level II, Order No. 0350 - Product Usage: The kit is used as a test for patients to monitor their cortisol and cortisone levels.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Devices)·Z-0512-2021·2020-12-09
Talladium Luminesse ML PMMA Milling Blank Recall for Incorrect Label
Talladium Inc is recalling 10 units of Luminesse ML PMMA milling blanks due to incorrect labels that may cause compatibility issues with milling machines.
Product
Luminesse ML PMMA, 98x20mm, REF: 5336-B1 - Product Usage: used as a milling blank in the fabrication of provisional crowns and bridges. All blanks are solely used by a Trained Dental Technician or on the order of a dental professional.
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0119-2021·2020-12-09
Teligent Pharma Recalls Clobetasol Propionate Ointment Due to Potency Issues
Teligent Pharma is recalling Clobetasol Propionate Ointment 0.05% because some tubes have superpotent or subpotent assay results.
Product
Clobetasol Propionate Ointment USP 0.05%, Net Wt. 50 grams, Rx Only, Teligent Pharma. Inc. Buena, NJ 08310 NDC 52565-039-60
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0115-2021·2020-12-09
InvaTech Recalls Levocetirizine Dihydrochloride Tablets Due to Stability Failure
InvaTech Pharma Solutions is recalling specific lots of Levocetirizine Dihydrochloride Tablets 5 mg because one lot failed stability testing.
Product
Levocetirizine Dihydrochloride Tablets, USP, 5 mg 30-count bottle, Rx Only, Distributed by: Marlex Pharmceuticals, Inc. New Castle, DE 19720. NDC 10135-0639-30
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·20V759000·2020-12-08
Nissan Recalls 2020 Titan Trucks Due to Engine Wiring Fire Risk
Nissan is recalling 2020 Titan and Titan XD trucks because an exposed wire in the engine harness could cause an electrical short, leading to engine stall or fire.
Product
NISSAN — NISSAN TITAN
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V757000·2020-12-08
Grand Design Recalls 2020 Transcend Trailers Due to Gas Leak Risk
Grand Design is recalling 2020 Transcend recreational trailers because a gas leak at the cook stove joint may increase the risk of fire.
Product
GRAND DESIGN — GRAND DESIGN TRANSCEND
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V756000·2020-12-08
2019 Mercedes-Benz Sprinter Vehicles Recalled for Inaccurate Operator's Manual
Daimler Vans USA is recalling 2019 Mercedes-Benz Sprinter vehicles because the provided operator's manual may contain inaccurate or incomplete safety information.
Product
FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 4500, SPRINTER 3500, SPRINTER 1500, SPRINTER 2500
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V758000·2020-12-08
McNeilus Recalls 2020 Bridgemaster V Mixers Due to Missing Axle Information
McNeilus is recalling 2020 Bridgemaster V Mixer trucks because the required pusher axle operating position is missing from the information plate, increasing crash risk.
Product
MCNEILUS — MCNEILUS BRIDGEMASTER V MIXER
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·20V755000·2020-12-07
Infiniti Recalls M56, Q70, and Hybrid Models for Driveshaft Defect
Nissan is recalling specific Infiniti models because a broken driveshaft can cause loss of propulsion or disable the parking brake, increasing crash risk.
Product
INFINITI — INFINITI M56, Q70, M35 HYBRID, Q70 HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20E089000·2020-12-07
Curt Manufacturing Recalls Securelatch Adjustable Pintle Mounts Due to Fracture Risk
Curt Manufacturing is recalling Securelatch Adjustable Pintle Mounts because the 2-inch shank may fracture while hauling, increasing the risk of a crash.
Product
EQUIPMENT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V754000·2020-12-07
2021 East to West Recreational Trailers: Stowed Grill Fire Hazard
Forest River is recalling 2021 East to West recreational trailers (approximately 115 units). The grill can be stowed with the propane hose attached and burners on, which can increase fire risk.
Product
EAST TO WEST — EAST TO WEST DELLA TERRA, SILVER LAKE
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V753000·2020-12-04
Mercedes-Benz A 220 Recalled for Missing Tire Pressure Labels
Mercedes-Benz is recalling 2019 A 220 vehicles because missing tire pressure labels may lead to incorrect inflation and increased crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ A 220
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V752000·2020-12-04
E-One Recalls Emergency Vehicles Due to Display Lockup Risk
E-One is recalling specific 2019-2021 emergency vehicles because LCD displays may lock up, potentially delaying emergency efforts.
Product
E-ONE — E-ONE COMMERCIAL, QUEST II, TYPHOON N, CYCLONE II
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·20V751000·2020-12-03
Land Rover Recalls 2020 Models for Speedometer Display Software Error
Land Rover is recalling 2020 Discovery Sport and Range Rover Evoque vehicles because a software error may cause the speedometer to randomly switch units, potentially distracting drivers.
Product
LAND ROVER — LAND ROVER RANGE ROVER EVOQUE, DISCOVERY SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·21711·2020-12-03
Honda Recalls Pioneer 700 and 1000 Vehicles Due to Steering Control Issues
American Honda is recalling approximately 118,600 Pioneer 700 and 1000 vehicles because the electric power steering system may lose control, posing crash and injury hazards.
Product
Honda Pioneer 700 & 1000 Recreational Off-Highway Vehicles (ROVs) with Electric Power Steering (EPS)
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0497-2021·2020-12-02
Flexicare ProVu Video Stylet Recalled for Potential Airway Occlusion
Flexicare Medical Ltd. is recalling ProVu Single Use Video Stylets with ET Tubes because over-inflated cuffs may block the airway, making it difficult to ventilate patients.
Product
ProVu Single Use Video Stylet with ET Tube, Part/Size: 038-990-080U/ 8.0, 038-990-075U/ 7.5, 038-990-070U/ 7.0, 038-990-065U/ 6.5 *Note: product list updated per 12/23/2020 letter to customers
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0103-2021·2020-12-02
Paroex Oral Rinse Recalled for Burkholderia lata Contamination
Sunstar Americas is recalling Paroex Oral Rinse due to microbial contamination with Burkholderia lata. The recall covers specific lots distributed nationwide.
Product
Paroex (chlorhexidine gluconate) Oral Rinse, USP 0.12%, Alcohol Free, Rx only, packaged in: a) 1 pint (473 mL) NDC 52376-021-02; b) 4 fl oz (118 mL) NDC 52376-021-04, Sunstar Americas, Inc.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0484-2021·2020-12-02
Hill-Rom Recalls Life2000 Ventilation Systems Due to Fire Risk
Hill-Rom is recalling 67 Life2000 Ventilation Systems because they pose a risk of fire under certain conditions. The devices are used in home and institutional settings.
Product
Life2000 Ventilation System, including Life2000 Ventilator and Life2000 Compressor, Model MS-01-0118 - Product Usage: use in home and institutional settings and is not intended for ambulance or air transport.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·20V750000·2020-12-02
Kia Recalls 294,756 Vehicles for Engine Compartment Fire Risk
Kia is recalling 294,756 vehicles from 2011-2015 due to a risk of engine compartment fire while driving. Dealers will inspect for leaks and update software.
Product
KIA — KIA FORTE KOUP, SOUL, FORTE, SORENTO
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0491-2021·2020-12-02
FDA Recalls Geistlich Bio-Oss Pen Due to Granule Expulsion Risk
Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen units because granules may be expelled all at once, posing a risk of tissue injury.
Product
Geistlich Bio-Oss Pen 0.25-1mm 0.5g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20116
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·20V749000·2020-12-02
Audi 2021 A6, Q7, RS6, and RS7 Crash Sensor Electrical Defect
Volkswagen Group of America (Audi) is recalling 2021 Audi A6, Q7, RS6, and RS7 vehicles. An electrical connector can detach from door crash sensors, potentially delaying restraint system activation during side-impact crashes.
Product
AUDI — AUDI RS 6 AVANT, RS 7, A6, Q7
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0483-2021·2020-12-02
Bayer Recalls MEDRAD Stellant FLEX Syringe Kits Due to Cracks
Bayer Medical Care is recalling specific lots of MEDRAD Stellant FLEX 150 mL syringe kits because they may have holes or cracks that allow fluid to leak.
Product
Brand Name: MEDRAD Stellant FLEX Syringe Kits Common Name: Angiographic Syringe Catalog/REF Number: FLEXD-150-SCS Description: 2 - 150 mL FLEX syringes, 1 large saline spike, 1 small contrast spike, patient t-connector tubing & prime tube. Catalog/REF Number…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0482-2021·2020-12-02
ViewRay MRIdian Linac System Recalled for Potential Burn Injury Risk
Viewray, Inc. is recalling 35 ViewRay MRIdian Linac Systems because receive coil components may reach elevated temperatures, posing a risk of burn injury to patients or users.
Product
ViewRay MRIdian Linac System: Model No. 20000, CE, Rated Supply Voltage - 380/480 VAC, 3 - Frequency Range (Hertz) - 50/60 Hz, Rated Input in Amperes - 210 A, UDI. The MRIdian system and the MRIdian Linac system, with magnetic resonance imaging capabilities, is intended to…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0492-2021·2020-12-02
Geistlich Bio-Oss Pen Recalled Due to Granule Expulsion Risk
Geistlich Pharma North America is recalling Geistlich Bio-Oss Pen 1-2mm 0.5g units because granules may be expelled all at once, posing a risk of tissue injury.
Product
Geistlich Bio-Oss Pen 1-2mm 0.5g - Product Usage: natural bone mineral for filling of bone defects in maxillofacial surgery, implantology, and periodontology. Product Number: 20126
Category
Medical Device
Distribution
Distributed nationwide