Product Recalls in Virginia

Product recalls affecting Virginia — including food, drugs, consumer products, medical devices, and vehicles distributed to Virginia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,803 recalls have been distributed to Virginia in the last 12 months.

53,829 total recalls
2,803 in last 12 months

Showing 95619580 of 53,829 recalls

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

Recalled Item: ICD CROME DR MRI IS1 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-DR DDBB1D4 EVERA XT IS1/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: CRTD COBALT XT HF MRI IS1 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-DR DDBB1D1 EVERA XT IS1/DF1 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-DR DDMB2D4 EVERA MRI XT IS-1/DF4 INT 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 DVBC3D1 EVERA S IS1/DF1 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: ICD-VR DVFC3D1 VISIA AF 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: CRTD DTMB2Q1 AMPLIA 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: ICD-VR DVBB1D4 EVERA XT 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: CRTD VIVA QUAD XT CUST PARY GOLD 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 COBALT 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 COBALT HF MRI IS1 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: CRT-D DTBA1D4 VIVA XT 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: CRTD DTMC2D4 COMPIA 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: ICD-VR DVBB1D1 EVERA XT IS1/DF1 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-DR DDMB2D1 EVERA MRI XT 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: CRT-D DTBB2D1 VIVA S IS1/DF1 INTL 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 DTMC2D1 COMPIA 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 COBALT XT DR 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 DTMB1Q1 AMPLIA MRI QUAD 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