Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
2,678 in last 12 months

Showing 64616480 of 29,298 recalls

Medical DeviceMay 10, 2023· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: ICD-VR DVMD3D4 PRIMO MRI 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: CRT-D VIVA QUAD XT 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· Medtronic Inc., Cardiac Rhythm and Heart Failure (CRHF)

Recalled Item: CRTD COBALT HF QUAD MRI IS4 DF1 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 DTMA2D4 CLARIA MRI OUS 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 DTMA1D1 CLARIA MRI US DF1 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 DTMB2D1 AMPLIA MRI OUS DF1 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 DVMC3D1 EVERA MRI S OUS/US 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: ICD-VR DVEX3E4 EV ICD EV4 PIVOTAL 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: CRT-D DTBB1D4 VIVA S IS1/DF4 US 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: CRT-D DTBB1D1 VIVA S IS1/DF1 US 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: CRT-D DTBA2D1 VIVA XT IS1/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 DTBA2D1G VIVA XT IS1 DF1 OUS GOLD 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 DVME3D1 MIRRO MRI 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: CRT-D DTBB2QQ VIVA QUAD S IS4/DF4 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 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 DDME3D1 MIRRO MRI 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 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 COBALT XT HF QUAD MRI IS4 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 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