Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 2101–2120 of 52,120 recalls
Recalled Item: DreamStation Auto BiPAP. Non-Continuous Ventilator. Recalled by Philips...
The Issue: Devices may possess a programming error resulting in an incorrect device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DreamStation Auto. Non-Continuous Ventilator. Recalled by Philips...
The Issue: Devices may possess a programming error resulting in an incorrect device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: PERLA ¿ TL MIS Product Name: CANNULATED FENESTRATED Recalled by...
The Issue: Cannulated fenestrated polyaxial screws may be incorrectly labeled
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DreamStation Auto CPAP. Non-Continuous Ventilator. Recalled by Philips...
The Issue: Devices may possess a programming error resulting in an incorrect device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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.