Product Recalls in Nebraska

Product recalls affecting Nebraska — including food, drugs, consumer products, medical devices, and vehicles distributed to Nebraska. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,095 recalls have been distributed to Nebraska in the last 12 months.

49,150 total recalls
1,095 in last 12 months

Showing 6361–6380 of 28,140 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 12, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline O.R. Scissors Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: The scissors were manufactured without a tip protector resulting in the...

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 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 12, 2023· Ossur H / F

Recalled Item: Icelock 125 Ratchet Recalled by Ossur H / F Due to A mechanical lock used to...

The Issue: A mechanical lock used to connect and release a locking liner into a...

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

Recalled Item: CRTD DTMB2QQ AMPLIA 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