Product Recalls in Montana

Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,535 recalls have been distributed to Montana in the last 12 months.

48,326 total recalls
2,535 in last 12 months

Showing 64016420 of 27,852 recalls

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: 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: 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: 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· 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 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: 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-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: 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 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: 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 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: 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: 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: CRT-D DTBA2D4 VIVA XT IS1/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· BearCare, Inc.

Recalled Item: Walnut Wearable Smart Thermometer Recalled by BearCare, Inc. Due to There...

The Issue: There have been reports of skin burns to children wearing the device.

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 9, 2023· Virtual Radiologic Corp.

Recalled Item: vRad PACS with Mammography Recalled by Virtual Radiologic Corp. Due to The...

The Issue: The error resulted in intermittent failure of current (primary) radiology...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· BioFire Diagnostics, LLC

Recalled Item: BioFire Respiratory Panel 2.1 (RP2.1) Recalled by BioFire Diagnostics, LLC...

The Issue: Due to manufacturing issue, panels may result in false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· BioFire Diagnostics, LLC

Recalled Item: FilmArray Pneumonia Panel (Pneumo) Recalled by BioFire Diagnostics, LLC Due...

The Issue: Due to manufacturing issue, panels may result in false negative results.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 8, 2023· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Calibrator Kit 20-in vitro diagnostic use only....

The Issue: Potential to cause biased results in the upper end of the reportable range...

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

Class II — Potential Health HazardOngoing