Product Recalls in Colorado
Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,191 recalls have been distributed to Colorado in the last 12 months.
Showing 2141–2160 of 51,434 recalls
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: Omeprazole Delayed-release Capsules Recalled by Dr. Reddy's Laboratories,...
The Issue: Presence of foreign tablets/capsules: presence of foreign Divalproex Sodium...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Budesonide Inhalation Suspension Recalled by Cipla USA, Inc. Due to Lack of...
The Issue: Lack of Assurance of Sterility: A market complaint was received for leakage...
Recommended Action: Stop taking this medication. Contact your pharmacy or 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: 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: 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 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: 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: 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: SmartPath to dStream for XR and 3.0T Model Numbers (REF): (1) 781270...
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 Model Numbers (REF): (1) 781315 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: Evolution Upgrade 1.5T Model Numbers (REF): (1) 782116 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: Intera 3.0T Quasar Dual Model Number (REF): 781150 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 7700 Model Numbers (REF): (1) 782120 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: Evolution Upgrade 3.0T Model Numbers (REF): (1) 782117 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 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: 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: 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.