Product Recalls in Iowa
Product recalls affecting Iowa — including food, drugs, consumer products, medical devices, and vehicles distributed to Iowa. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,627 recalls have been distributed to Iowa in the last 12 months.
Showing 6321–6340 of 28,127 recalls
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.
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.
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.
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.
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.
Recalled Item: Driver Instrument Recalled by Boston Scientific Neuromodulation Corporation...
The Issue: Pending update to indirect decompression system instructions for use...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.
Recalled Item: ICD-DR DDBB2D1 EVERA 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.
Recalled Item: ICD-DR DDMC3D1 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.
Recalled Item: ICD DDPA2D1G COBALT XT DR MRI DF1 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.
Recalled Item: CRT-D DTBB2D4 VIVA S IS1/DF4 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.
Recalled Item: CRT-D DTBA2QQ VIVA QUAD XT 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.
Recalled Item: CRT-D DTBA1Q1 VIVA QUAD XT IS4/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.
Recalled Item: CRTD CROME 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.
Recalled Item: CRTD DTMA2D1 CLARIA 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.
Recalled Item: CRTD DTMC1D1 COMPIA 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.
Recalled Item: CRTD DTMB1D4 AMPLIA MRI 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.
Recalled Item: ICD-VR VISIA AF S US/OUS IS1/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.
Recalled Item: CRT-D DTBC2QQ BRAVA QUAD 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.
Recalled Item: ICD COBALT XT HF QUAD OUS 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.