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.

15551–15575 of 75897

HighFDA (Devices)·Z-2064-2023·2023-07-12
Surgical drill guides may bend and produce metal shavings during use
T.A.G. MEDICAL PRODUCTS CORPORATION is recalling Betta Link LG Reusable ProngED Guides used in orthopedic surgery because the guides may bend when force is applied, creating metal shavings that could injure patients.
Product
Betta Link LG Reusable ProngED Guide - Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045156
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2094-2023·2023-07-12
BD Pyxis CII Safe Dispensing Cabinets Recalled for Electrical Current Leakage
BD Pyxis CII Safe automated dispensing cabinets may leak excessive electrical current when connected to multi-socket power strips, risking electric shock and system downtime.
Product
BD Pyxis CII Safe, Software: V7, REF: 107-96, 107-97, 107-97-201; BD Pyxis CII Safe, Software: V7, REF: 107-223, 107-224, 111-191, 111-192, 111-193, 111-194, 111-195, 111-196, 111-197, 111-198; BD Pyxis CII Safe, Software: V8, 111-199-01, 111-200-01, 111-201-01, 111-202-01…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2082-2023·2023-07-12
Dermal repair scaffold recalled due to endotoxin testing failures
TEI Biosciences is recalling 10,159 units of PriMatrix Ag Meshed dermal repair scaffolds due to testing failures that cannot verify endotoxin levels. Procedures for testing bacterial toxin levels during manufacturing quality control were found to be flawed.
Product
PriMatrix Ag Meshed; Dermal Repair Scaffold; Rx Only; Sizes 10x12 cm (2:1), 10x25 cm (2:1), 20x25 cm (1:1), 4x4 cm (2:1), 6x6 cm (2:1), 8x12 cm (2:1), 8x8 cm (2:1).
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2091-2023·2023-07-12
Aptio Storage and Retrieval Module firmware error may cause incorrect test results
Siemens Aptio Automation Storage and Retrieval Module has a firmware error that may incorrectly associate test results to patient samples, potentially leading to incorrect patient results. Eighty-three units are affected worldwide.
Product
Aptio Automation Storage and Retrieval Module (SRM)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0895-2023·2023-07-12
Losartan Potassium Tablets Recalled for Blue Plastic Contamination
Strides Pharma Inc. is recalling Losartan Potassium Tablets, 25 mg, due to the presence of blue plastic pieces embedded in tablets from lot 7901903A. No illnesses or injuries have been reported.
Product
LOSARTAN POTASSIUM — LOSARTAN POTASSIUM (LOSARTAN POTASSIUM)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2080-2023·2023-07-12
PriMatrix Ag Dermal Repair Scaffold Recalled for Endotoxin Testing Issues
TEI Biosciences is recalling 1,689 units of PriMatrix Ag dermal repair scaffolds distributed nationwide due to potential endotoxin testing deficiencies. Testing procedures may not have been conducted reliably.
Product
PriMatrix Ag; Dermal Repair Scaffold; Rx Only; Sizes 10x12 cm, 10x25 cm, 20x25 cm, 4x4 cm, 6x6 cm, 8x12 cm, 8x8 cm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2058-2023·2023-07-12
Treadmill recalled for drive PCB malfunction causing unexpected acceleration
Full Vision Inc recalls 95 TRACKMASTER GE T2100-ST2 treadmills with a defective drive PCB that may misread signals, causing the equipment to unexpectedly stop, reverse, or accelerate forward.
Product
TRACKMASTER, TREADMILL GE T2100-ST2 220V CHINA, MODEL NUMBER 317-07927GE CHINA
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2086-2023·2023-07-12
Medical procedure packs recalled for compromised package seals
DeRoyal Industries is recalling 4,225 custom medical procedure packs nationwide because outer package seals may be open or compromised, potentially affecting sterility of the surgical materials inside.
Product
Custom medical procedure packs labeled as: a) OPEN HEART TRACECART, REF '53-1941; b) CARDIAC CATH PACK, REF '89-10045; c) SHOULDER PACK, REF '89-10115; d) MINOR ORTHO PACK, REF '89-10213; e) TOTAL KNEE PACK PGYBK, REF '89-10505; f) ANTERIOR HIP PACK PGYBK, REF…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2072-2023·2023-07-12
SurgiMend 2.0 Collagen Matrix Recalled for Endotoxin Testing Issues
TEI Biosciences is recalling SurgiMend 2.0 collagen matrices nationwide due to possible out-of-specification endotoxin test results from issues with in-process and finished goods testing procedures.
Product
SurgiMend 2.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 16x20 cm, 13x25 cm, 25x40 cm, 20x30 cm, 20x20 cm, 20x25cm, 10x15cm Semi-Oval,
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V477000·2023-07-12
Jayco Seneca recreational vehicles recalled for windshield wiper linkage failure
Jayco is recalling certain 2021-2022 Seneca recreational vehicles because the windshield wiper arms may fail, reducing driver visibility and increasing crash risk. Owners should contact Jayco customer service at 1-800-283-8267 for a free inspection and replacement.
Product
JAYCO — JAYCO, ENTEGRA SENECA, SENECA PRESTIGE, ACCOLADE XL, ACCOLADE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2069-2023·2023-07-12
SurgiMend soft tissue collagen matrix recalled for endotoxin testing verification issues
TEI Biosciences recalls 14,535 units of SurgiMend collagen matrices distributed nationwide due to potential endotoxin testing verification problems. Affected devices cannot be confirmed to meet endotoxin specifications.
Product
SurgiMend; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 1.0 5x6 cm, 1.0 6x12 cm, 1.0 10x10 cm, 1.0 10x15 cm, 1.0 10x20 cm, 1.0 16x20 cm, 1.0 13x25 cm, 1.0 4x16 cm, 1.0 3x3 cm, 1.0 4x7 cm, 1.0 4x12 cm, 1.0 6x16 cm, 1.0 25x40 cm, 1.0 20 x 30 cm, 1.0 8x16 cm, 1.0…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2054-2023·2023-07-12
TrackMaster Treadmill Recalled for Drive PCB Malfunction Risk
Full Vision Inc. is recalling 39 TrackMaster treadmills with a drive PCB malfunction that can cause unexpected stopping, reversal, or acceleration.
Product
TRACKMASTER, TREADMILL TMX428CP 110V, MODEL NUMBER 317-07928
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2061-2023·2023-07-12
BETTA LINK LG Implant Drill Guide Bending Risk
T.A.G. MEDICAL PRODUCTS is recalling BETTA LINK LG KNOTLESS IMPLANT KIT because drill guides may bend during surgical use, potentially creating metal shavings that could injure patients.
Product
BETTA LINK LG KNOTLESS IMPLANT KIT-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045160
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2088-2023·2023-07-12
Medical Procedure Packs with Compromised Package Seals Recalled
DeRoyal Industries is recalling 328 surgical procedure packs because outer package seals could be open or compromised, affecting product sterility. The affected packs are used in operating rooms nationwide.
Product
Custom medical procedure packs labeled as: a) STANDARD OB PACK ASCENSION WI, REF 89-10640 b) ANGIO PACK, REF 89-10901 c) BASIN, REF 89-1924 d) CYSTO PACK, REF 89-7133 e) TOTAL HIP PACK, REF 89-9134 f) EMERGENCY C-SECTION PACK, REF 89-9478
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2085-2023·2023-07-12
Soft tissue repair matrix recalled due to possible endotoxin contamination
TEI Biosciences is recalling 4,832 units of TissueMend Advanced Soft Tissue Repair Matrix due to possible out-of-specification endotoxin test results. No illnesses or injuries have been reported.
Product
TissueMend; Advanced Soft Tissue Repair Matrix; Rx Only; Sizes 5x6 cm, 6x10 cm, and 3x3 cm.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2066-2023·2023-07-12
LinkSymphoKnee Distal Femoral Augment Recalled for Improper Screw Placement
The LinkSymphoKnee Distal Femoral Augment is being recalled because fixation screws were inserted in the wrong direction during manufacturing. The improper placement could affect the implant's structural stability.
Product
LinkSymphoKnee Distal Femoral Augment - Tilastan - Size 7-8, Medial-Right/Lateral Left, 5mm- Intended for primary and revision total knee replacement in skeletally mature patients. Product Code: 880-307/11
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2068-2023·2023-07-12
OmniTom CT imaging device recalled for wheel loosening and battery contamination
NeuroLogica is recalling OmniTom CT imaging devices due to wheels that may loosen and battery boards that may be contaminated, both of which could prevent the device from operating properly and delay patient imaging.
Product
OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy that can be imaged in the 40 cm aperture, primarily head and neck Model Number: NL5000
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V481000·2023-07-12
2023 Nova Bus LFS Transit Buses Power Steering Hose Defect Recall
Nova Bus is recalling 2023 and 2022 LFS transit buses due to power steering hose assembly defects that could result in loss of steering assist and increased crash risk.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2055-2023·2023-07-12
TrackMaster Treadmill Drive PCB Malfunction Causes Unexpected Stop, Reverse, and Acceleration
Full Vision Inc is recalling 96 TrackMaster TMX428CP treadmills due to a drive PCB malfunction that can cause the belt to unexpectedly stop, reverse, or accelerate, posing an injury risk to users.
Product
TRACKMASTER, TREADMILL TMX428CP 220V, MODEL NUMBER 317-07929
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2052-2023·2023-07-12
Treadmill Recalled for Drive PCB Malfunction Causing Unexpected Belt Movement
Full Vision Inc is recalling approximately 565 TrackMaster TMX428 treadmills due to a drive circuit board malfunction that can cause the belt to unexpectedly stop, reverse, or accelerate, posing a risk of falls or injury.
Product
TRACKMASTER, TREADMILL TMX428 110V, MODEL NUMBER 317-07926
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2065-2023·2023-07-12
Betta Link LG Surgical Guide May Deform and Produce Metal Shavings
Betta Link LG surgical guides used in soft tissue and bone repair may bend under pressure during surgery, potentially releasing metal shavings that could injure patients. The manufacturer is recalling affected units in the U.S. and internationally.
Product
Betta Link LG Reusable Fishmouth Guide-Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045157
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V478000·2023-07-12
2021-2022 Toyota RAV4 Prime recalled for electrical fire risk
Toyota is recalling 43,442 2021-2022 RAV4 Prime and 2022 Lexus NX450H+ plug-in hybrid vehicles. A defective DC-DC converter electrical module can overheat and cause vehicle fire. Dealers will replace the component free of charge.
Product
LEXUS — LEXUS, TOYOTA NX450H+, RAV4 PRIME
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2062-2023·2023-07-12
Surgical drill guide may bend and produce metal shavings during use
T.A.G. Medical is recalling BETTA LINK SR surgical drill guides due to risk of bending and metal shavings during surgery.
Product
BETTA LINK SR REUSABLE PRONGED GUIDE- Intended for use in soft tissue to bone fixation in the repair of the natural ligament or tendon disruption or to assist in reconstruction surgeries. Part Number: 110045150
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·23V482000·2023-07-12
Nova Bus LFS Transit Buses Recalled for Driveshaft Separation
Nova Bus is recalling certain 2019-2023 LFS and LFS Artic transit buses. The transmission yoke may separate, causing driveshaft separation and sudden loss of drive power, increasing the risk of crashes and passenger injury.
Product
NOVA BUS — NOVA BUS LFS, LFS ARTIC
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2074-2023·2023-07-12
SurgiMend 3.0 Soft Tissue Graft Recalled for Endotoxin Testing Defect
SurgiMend 3.0 collagen matrix is being recalled nationwide (13,390 units) due to possible endotoxin contamination from deficiencies in endotoxin testing procedures.
Product
SurgiMend 3.0; Collagen Matrix for Soft Tissue Reconstruction; Rx Only; Sizes 5x6 cm, 6x12 cm, 10x15 cm, 16x20 cm, 13x25 cm, 25x40 cm, 20x30 cm, 20x20 cm, 20x25 cm, 1x5 cm, 10x25 cm 4x7cm Fenestrated, and 10x25 cm Fenestrated.
Category
Medical Device
Distribution
Distributed nationwide