Product Recalls in Kansas

Product recalls affecting Kansas — including food, drugs, consumer products, medical devices, and vehicles distributed to Kansas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,090 recalls have been distributed to Kansas in the last 12 months.

50,117 total recalls
1,090 in last 12 months

Showing 6361–6380 of 28,538 recalls

Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 12, 2023· Full Vision Inc

Recalled Item: TRACKMASTER Recalled by Full Vision Inc Due to Treadmill malfunction: drive...

The Issue: Treadmill malfunction: drive PCB can misread the signals and stop or reverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRT-D DTBB2Q1 VIVA QUAD S IS4/DF1 INTL Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD DTPA2D1G COBALT XT HF QUAD OUS Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD COBALT VR MRI IS1 DF1 Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD-DR DDMB1D4 EVERA MRI XT IS-1/DF4 US Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD-VR DVAB1D4 VISIA AF US DF4 Recalled by Medtronic Inc., Cardiac Rhythm...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD CROME HF QUAD MRI IS4 DF4 Recalled by Medtronic Inc., Cardiac Rhythm...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD-VR DVAB1D1 VISIA AF US IS1/DF1 Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRT-D DTBC2Q1 BRAVA QUAD IS4/DF1 INTL Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD COBALT XT VR MRI DF4 Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD CROME VR MRI DF4 Recalled by Medtronic Inc., Cardiac Rhythm and Heart...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD EVERA XT DR GOLD CTD Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Fresenius Kabi USA, LLC

Recalled Item: LVP software of the Ivenix Infusion System (IIS) Recalled by Fresenius Kabi...

The Issue: Retroactively reported corrections from 2023: 1) A software defect may cause...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD COBALT XT HF MRI IS1 DF1 Recalled by Medtronic Inc., Cardiac Rhythm and...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD DTPA2D1PX COBALT XT HF QUAD OUS Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD COBALT VR MRI DF4 Recalled by Medtronic Inc., Cardiac Rhythm and Heart...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD-DR DDMC3D4 EVERA MRI S IS-1/DF4 GLOB Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD DTMA2Q1 CLARIA MRI QUAD OUS DF1 Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD DTMA2QQ CLARIA MRI QUAD OUS DF4 Recalled by Medtronic Inc., Cardiac...

The Issue: There is a rare potential for reduced- or no-energy output during high...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing