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. 2,660 recalls have been distributed to Iowa in the last 12 months.
Showing 2081–2100 of 49,990 recalls
Recalled Item: Ingenia Elition X Model Numbers (REF): (1) 781358 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to dStream for 3.0T Model Number (REF): 782145 Recalled by Philips...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 1.5T S Model Number (REF): 781347 Recalled by Philips North America...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T Model Numbers (REF): (1) 781342 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MR 5300 Model Numbers (REF): (1) 782110 Recalled by Philips North America...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S Model Numbers (REF): (1) 781359 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 3.0T Recalled by Philips North America Due to The potential for...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Upgrade to MR 7700 Model Number (REF): 782130 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia 3.0T CX Model Numbers (REF): (1) 781271 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Elition S Model Numbers (REF): (1) 781357 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva XR Recalled by Philips North America Due to The potential for...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartPath to Ingenia Elition X Model Numbers (REF): (1) 782118 Recalled by...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura R8.2.x Systems. Software Verion: R8.2.x. 1. Allura Xper FD10...
The Issue: Potential for temporary loss of imaging (X-ray) functionality due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HeartSine SAM 350P Recalled by HeartSine Technologies Ltd Due to Due to a...
The Issue: Due to a component manufacturing issue, Automated External Defibrillator may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition X Model Numbers (REF): (1) 781356 Recalled by Philips North...
The Issue: The potential for component failures in the Gradient Coil of the affected MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laser light show projectors manufactured by BLS Recalled by Beyond Laser...
The Issue: The remote interlock connector, which is required by 21 CFR 1040.10(f)(3),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Crumbled Cookie Bar (85200) Recalled by Rich Ice Cream Co Due to Potential...
The Issue: Potential Listeria Monocytogenes Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cool Watermelon Bar (86270) Recalled by Rich Ice Cream Co Due to Potential...
The Issue: Potential Listeria Monocytogenes Contamination
Recommended Action: Do not consume. Return to store for a refund or discard.