Product Recalls in South Dakota
Product recalls affecting South Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to South Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,512 recalls have been distributed to South Dakota in the last 12 months.
Showing 9461–9480 of 47,632 recalls
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Daytrana (methylphenidate transdermal system) CII Recalled by Noven...
The Issue: Defective Delivery System: Out of specification for shear.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VITROS 5600 Integrated System- For use in the in vitro quantitative Recalled...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System - For use in the in vitro quantitative...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System - . For use in Recalled by Ortho-Clinical...
The Issue: MicroTip Pack Opener Assembly Potentially Not Removing or Replacing MicroTip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Storage and Retrieval Module (SRM)-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Input Output Module (IOM) FLX-201-Laboratory Automation system Brand names...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vesmatic Cube 80 Interface Module (VMC)-Laboratory Automation system Brand...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PVT Interface Module (PVT)-Laboratory Automation system Brand names of the...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alinity h Interface Module (HSQ)-Laboratory Automation system Brand names of...
The Issue: Firmware versions have the potential to mis-associate sample IDs leading to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JARDIANCE (Empagliflozin) Recalled by Boehringer Ingelheim Pharmaceuticals,...
The Issue: Labeling: Label Mix-up
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dofetilide Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...
The Issue: Failed Content Uniformity Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DEVILBISS HEALTHCARE 1025 SERIES OXYGEN CONCENTRATOR Recalled by DeVilbiss...
The Issue: The instruction manual is being replaced with an updated version that is in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Anti-SARSCoV- 2 Total N Antibody...
The Issue: Incorrect Number of Calibrator Levels (2) Set for the VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost C50 -intended for use in generating radiographic...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DigitalDiagnost C50 1.1-intended for use in generating radiographic images...
The Issue: If the PM for the telescopic carriage is not performed annually as defined...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEKTOVI (binimetinib) tablets Recalled by Pfizer Inc. Due to Labeling:...
The Issue: Labeling: Incorrect or Missing Lot and/or Exp Date: The carton and bottle...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: AQURE Software Versions 2.5.2 2.5.3 2.5.4 2.6.0 2.6.1 Recalled by Radiometer...
The Issue: Due to potential software issue that may result in patient mix-up information.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.