State

South Dakota product recalls

73,213 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: 567
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 567 (21%) are Severe.

Which agencies issued them

These figures cover only the 2,684 recalls whose distribution notice names South Dakota specifically. The 73,213 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

15576–15600 of 75897

HighFDA (Devices)·Z-2090-2023·2023-07-12
Custom Medical Procedure Packs Recalled for Compromised Package Seals
DeRoyal Industries is recalling 306 custom medical procedure packs because the outer package seals could be open or compromised, affecting the sterility of the contents. Affected packs were distributed nationwide.
Product
Custom medical procedure packs labeled as: a) CATH ANGIOGRAPHY DRAPE PACK, REF 89-7102; b) CHOLANGIOGRAPHY KIT, REF 89-7322; c) CATH LAB PACK, REF 89-9183
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2083-2023·2023-07-12
Revize Collagen Matrix Recalled for Potential Endotoxin Testing Issues
TEI Biosciences recalls 199 units of Revize Collagen Matrix due to possible out-of-specification endotoxin test results from faulty testing procedures. The product is distributed nationwide.
Product
Revize; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 10x10 cm, 4x12 cm, 4x16 cm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2075-2023·2023-07-12
SurgiMend 4.0 Collagen Implants Recalled for Endotoxin Testing Failures
TEI Biosciences is recalling 5,664 units of SurgiMend 4.0 soft tissue reconstruction implants nationwide due to issues with endotoxin testing that may have resulted in out-of-specification test results.
Product
SurgiMend 4.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 13x25 cm, 25x40 cm, 20x30 cm, 10x25 cm, 20x0.5 cm, and 10x25 cm Fenestrated.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2079-2023·2023-07-12
Dermal Repair Scaffold Recalled Due to Endotoxin Testing Issues
TEI Biosciences is recalling PriMatrix Meshed dermal repair scaffolds due to endotoxin testing failures. The recall affects 33,277 units distributed nationwide.
Product
PriMatrix Meshed; Dermal Repair Scaffold; Rx Only; Sizes 20x25 cm (1:1), 3x3 cm (2:1), 4x4 cm (2:1), 5x5 cm (2:1), 6x6 cm (2:1), 8x12 cm (2:1), and 8x8 cm (2:1).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1224-2023·2023-07-12
Havasu Beetroot Powder Recalled for Undeclared Milk Allergen
Havasu Beetroot Powder (11.5 oz.) is being recalled because it contains undeclared milk. Consumers with milk allergies who consume this product may experience allergic reactions.
Product
Havasu Beetroot Powder, 11.5 oz.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2078-2023·2023-07-12
PriMatrix Dermal Scaffold Recalled Due to Endotoxin Testing Issues
TEI Biosciences is recalling 30,528 units of PriMatrix Fenestrated dermal repair scaffolds due to possible out-of-specification endotoxin test results. The FDA Class II recall affects wound healing products distributed nationwide.
Product
PriMatrix Fenestrated; Dermal Repair Scaffold; Rx Only; Sizes 4x4 cm, 6x6 cm, 8x8 cm, 14mm Disc, 18mm Disc, 2x2 cm, and 10x25 cm (Meshed 2:1).
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2071-2023·2023-07-12
SurgiMend collagen matrices recalled for endotoxin test result quality issues
TEI Biosciences recalls SurgiMend 1.0 collagen matrices due to problems with endotoxin testing procedures that may have produced inaccurate test results. 52 units were distributed nationwide.
Product
SurgiMend 1.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 18x12 cm Thin and 10x15 cm Thin.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0894-2023·2023-07-12
Tizanidine tablets recalled nationwide for failed stability specifications
Preferred Pharmaceuticals is recalling 541 bottles of Tizanidine 4mg tablets nationwide due to failed stability specifications. Consumers with affected lot numbers should contact their pharmacist or healthcare provider.
Product
TIZANIDINE — TIZANIDINE (TIZANIDINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2095-2023·2023-07-12
Teleflex Pilling O'Reilly Esophageal Retractor Recalled for Incomplete Cleaning Instructions
TELEFLEX LLC recalled the Pilling O'REILLY ESOPHAGEAL RETRACTOR (REF 381801A) due to incomplete pre-cleaning instructions in the product's Instructions for Use. The recall affects 365 units distributed nationwide and internationally.
Product
Pilling O'REILLY ESOPHAGEAL RETRACTOR, REF 381801A; ENT retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2084-2023·2023-07-12
Collagen matrix recalled for endotoxin testing methodology issues
TEI Biosciences recalled 665 units of Revize-X collagen matrix nationwide due to possible out-of-specification endotoxin test results caused by issues with the company's testing procedures. No illnesses have been reported.
Product
Revize-X; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 12x6 cm and 10x9 cm.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0892-2023·2023-07-12
Prescription Drug Tizanidine Tablets Recalled for Failed Dissolution Specifications
Amerisource Health Services LLC recalls approximately 4,971 cartons of Tizanidine Tablets due to failed dissolution specifications. Tablets that do not dissolve properly may not provide intended therapeutic benefit.
Product
TIZANIDINE — TIZANIDINE (TIZANIDINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2096-2023·2023-07-12
Teleflex Surgical Retractor Recalled for Incomplete Pre-Cleaning Instructions
Teleflex LLC is recalling 170 units of the Pilling Lowsley Prostatic Retractor due to incomplete pre-cleaning instructions in the user manual. Incomplete instructions may prevent proper sterilization of the surgical instrument.
Product
Pilling LOWSLEY PROSTATIC TRACTOR CVD, REF 243200; retractor
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2093-2023·2023-07-12
COVID-19 Test Strips Recalled for Lot Number Label Discrepancy
NeuMoDx SARS-CoV-2 test strips from lot 123909 have conflicting lot numbers between the package label and barcode label that the instrument reads.
Product
NeuMoDx SARS-CoV-2 Assay -IVD intended for the qualitative detection of SARS-CoV-2 RNA from nasal, nasopharyngeal and oropharyngeal swabs in transport medium and bronchoalveolar lavage (BAL) specimens from individuals suspected of COVID-19 by their healthcare provider (HCP).…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V474000·2023-07-11
Prevost H3-45 Turn Signal Light Failure Increases Crash Risk
Prevost is recalling 2022-2024 H3-45 and H3-45 VIP vehicles because the right front turn signal light may fail when activated. Inoperative turn signals and hazard lights reduce visibility to other drivers and increase crash risk.
Product
PREVOST — PREVOST H3-45 VIP, H3-45
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V475000·2023-07-11
Prevost Recalls X3-45 Commuter Buses Due to Seat Bolt Loosening
Prevost is recalling 2021 and 2023 X3-45 Commuter buses because a seat bolt may loosen, leaving the seat back unsecured and increasing crash injury risk.
Product
PREVOST — PREVOST X3-45 COMMUTER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V485000·2023-07-11
2023 Toyota RAV4 Recalled for Improperly Installed Tire Valve Stems
Gulf States Toyota is recalling 195 2023 Toyota RAV4 vehicles equipped with 17" black alloy wheels. The tire valve stems may be improperly installed or damaged, potentially causing air leakage, underinflation, and crash risk.
Product
TOYOTA — TOYOTA RAV4
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23E053000·2023-07-11
Seats Incorporated Recalls Passenger Flip Seats Due to Missing Safety Clip
Seats Incorporated is recalling specific passenger flip-up seats that may be missing a safety clip, which could allow the seat to fall and cause injury.
Product
SEATS:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V472000·2023-07-10
Yamaha Recalls 2022 Tenere 700 Motorcycles Due to Brake Caliper Bolt Defect
Yamaha is recalling 2022 Tenere 700 motorcycles because front brake caliper bolts may have incorrect thread lengths, risking brake failure.
Product
YAMAHA — YAMAHA TENERE 700
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V473000·2023-07-10
Boreas Camper XT Travel Trailers Recalled for Gas Leak Risk
Boreas Campers is recalling 2021-2022 XT travel trailers because a cooktop component may fracture and cause a gas leak, increasing fire risk.
Product
BOREAS CAMPER — BOREAS CAMPER XT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V471000·2023-07-10
2023 BMW XM and 2024 X5-X7 vehicles recalled for knee air bag defect
BMW of North America is recalling 2023 XM and certain 2024 X5, X6, and X7 vehicles because the knee air bag may not have been manufactured correctly and could fail to deploy during a crash. Dealers will replace the air bag free of charge.
Product
BMW — BMW X5, X6, XM, X7
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23E052000·2023-07-10
Dana Spicer Driveshafts Recalled for Risk of Breaking Under Load
Dana Incorporated is recalling specific Dana-Spicer driveshafts that can break under certain loading conditions, potentially causing a loss of drive power and increasing crash risk.
Product
POWER TRAIN:DRIVELINE:DRIVESHAFT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23E051000·2023-07-07
Ironman 4x4 Recalls Pro Forge Upper Control Arms for Steering Loss Risk
Ironman 4x4 is recalling Pro Forge upper control arms because the ball joint may fail, causing loss of steering control.
Product
SUSPENSION:FRONT:CONTROL ARM:UPPER BALL JOINT recall
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V468000·2023-07-07
2023 Toyota Tundra Spare Tire Carrier May Detach Due to Insufficient Welds
Toyota is recalling certain 2023 Tundra, Tundra Hybrid, and Sequoia Hybrid vehicles due to insufficiently welded spare tire carrier assemblies that may break and allow the spare tire to detach, increasing crash risk.
Product
TOYOTA — TOYOTA TUNDRA HYBRID, TUNDRA, SEQUOIA HYBRID
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·23V469000·2023-07-07
Newmar motorhomes recalled for defective seat belt mounting brackets
Newmar is recalling certain 2019–2023 motorhomes because modified seat belt mounting brackets can fail to properly restrain occupants in a crash, violating federal safety standards.
Product
NEWMAR — NEWMAR BAY STAR, BAY STAR SPORT, SUPER STAR
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·23V467000·2023-07-06
Freightliner Recalls eCascadia Trucks for E-Axle Welding Defect
Daimler Trucks is recalling 2023-2024 Freightliner eCascadia vehicles because a defective e-axle weld may cause sudden loss of drive power, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER E-CASCADIA
Category
Vehicle
Distribution
Distributed nationwide