Go Backs

South Dakota Recalls

13,044 recalls distributed in South Dakota

per page
Chrysler (FCA US, LLC)
Medium RiskNHTSA

2024-2025 Jeep Wagoneer S and Dodge Charger Recalled for Display Failure

  • Distributed nationwide
  • Sold at Authorized FCA dealers, Jeep dealers +1 more
  • 20,271 units affected
Recalled
Added
Shyft
Medium RiskNHTSA

2022 Utilimaster Aeromaster Recalled for Incorrect Weight Rating Label

  • Distributed nationwide
  • Sold at authorized dealers
Recalled
Added
Biomerieux
Medium RiskFDA Device

VITEK 2 Gram-negative Susceptibility Cards Recalled for Testing Failures

  • Distributed nationwide
  • Sold at Direct distribution to laboratories and hospitals
  • 2,668,954 units affected
Updated
Recalled
Medium RiskFDA Device

Dimension Creatinine Flex Reagent Cartridges Recalled for Inaccurate Results

  • Distributed nationwide
  • Sold at Siemens Healthcare Diagnostics, Laboratory supply distributors
  • 18,080 units affected
Recalled
Added
SCOPE HEALTH
Medium RiskFDA Drug

Optase Dry Eye Intense Drops Recalled Due to Lack of Assurance of Sterility

  • Distributed nationwide
  • Sold at Retail pharmacies, Optical centers
Recalled
Added
Thea Pharma
Medium RiskFDA Drug

iVIZIA Lubricant Eye Drops Recalled for Lack of Sterility

  • Distributed nationwide
  • Sold at Retail pharmacies, Drug stores
Recalled
Added
American Regent
Low RiskFDA Drug

Levocarnitine Injection Recalled for Missing Labeling

  • Distributed nationwide
  • Sold at wholesalers, distributors
  • 74,040 units affected
Recalled
Added
Wells Pharma of Houston
Medium RiskFDA Drug

Wells Pharma Injectable Solutions Recalled for Quality Standard Deviations

  • Distributed nationwide
  • Sold at Hospitals, Infusion centers +1 more
  • 25,265 units affected
Recalled
Added
Hyundai Motor America
Medium RiskNHTSA

2025-2026 Hyundai Elantra and Tucson Recalled for Air Bag Sensor Defect

  • Distributed nationwide
  • Sold at Hyundai dealers
Recalled
Added
Tesla
Medium RiskNHTSA

2024-2026 Tesla Cybertruck Recalled for Wheel Stud Separation

  • Distributed nationwide
  • Sold at Tesla, Inc.
Recalled
Added
Volkswagen Group of America
Medium RiskNHTSA

2025-2026 Volkswagen Taos Recalled for Fuel Tank Leak After Crash

  • Distributed nationwide
  • Sold at authorized Volkswagen dealers
  • 38,710 units affected
Recalled
Added
B BRAUN MEDICAL
High RiskFDA Drug

B. Braun Sterile Water and Irrigation Bags Recalled for Sterility Risks

  • Distributed nationwide
  • Sold at Hospitals, Surgical centers +1 more
  • 220,836 units affected
Updated
Recalled
Philips North America
Medium RiskFDA Device

Philips MRE Scanning Systems Recalled for Accuracy Errors

  • Distributed nationwide
  • Sold at Authorized Philips medical equipment distributors, Direct sales to hospitals and clinics
Recalled
Added
Advanced Bionics
Medium RiskFDA Device

HiResolution Bionic Ear M Zn-Air Battery Paks Recalled for Battery Access Risk

  • Sold in 51 states
  • Sold at Authorized Medical Distributors, Audiology Clinics
  • 45,173 units affected
Recalled
Added
Q Straint
Medium RiskNHTSA

Q'Straint QRT-3 Wheelchair Retractors Recalled for Locking Defect

  • Distributed nationwide
  • Sold at Vehicle manufacturers, Authorized dealers
Recalled
Added
Medium RiskNHTSA

2025 Toyota RAV4 Recalled for Improperly Welded Seat Brackets

  • Distributed nationwide
  • Sold at authorized Toyota dealers
Recalled
Added
Medium RiskNHTSA

2027 Trails West RPM Freeride Trailers Recalled for Cooktop Fire Risk

  • Distributed nationwide
  • Sold at Trails West dealers
Recalled
Added
Zimmer
Medium RiskFDA Device

Disposable Mixing Bowls and Spatulas Recalled for Defective Package Seals

  • Sold in 31 states
  • Sold at Hospital suppliers, Medical device distributors
  • Ten complaints received regarding package seal issues; no specific injury counts provided.
Recalled
Added
Medtronic
High RiskFDA Device

Medtronic Sphere-9 Catheter Recalled Due to Heart Rhythm Interactions

  • Distributed nationwide
  • Sold at medical supply distributors, hospitals +1 more
  • Observations of ventricular fibrillation (VF) during therapy.
Recalled
Added
Milestone S.R.L.
Medium RiskFDA Device

Milestone VACUUM BAG SU LARGE Specimen Containers Recalled for Reagent Leakage

  • Distributed nationwide
  • Sold at authorized medical distributors
  • reagents contamination
Recalled
Added
Healthmark Industries
Medium RiskFDA Device

Mesh Style Tip Protectors Recalled for Lack of FDA Clearance

  • Distributed nationwide
  • Sold at Authorized distributors, Direct sales
  • 4,291,797 units affected
Recalled
Added
Boston Scientific
Critical RiskFDA Device

Boston Scientific Pacemakers and CRT-Ps Recalled for Software Update

  • Distributed nationwide
  • Sold at Hospitals, Medical Facilities +1 more
  • 1,404,232 units affected
Recalled
Added
Clinical Innovations
Medium RiskFDA Device

Kiwi Omni Vacuum Delivery System Recalled for Device Breakage Risk

  • Sold in 37 states
  • Sold at Hospital suppliers, Medical distributors
  • Complaints of device breakage; no specific injury counts provided.
Recalled
Added
Hologic
Medium RiskFDA Device

Genius Review Station Recalled Due to Misconfigured Display Settings

  • Distributed nationwide
  • Sold at Hologic, Inc., Authorized medical device distributors
Recalled
Added