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. 2,696 recalls have been distributed to Colorado in the last 12 months.
Showing 6021–6040 of 28,964 recalls
Recalled Item: HF Resection Electrodes - HF resection electrodes are part of Recalled by...
The Issue: Additional Caution statements in IFU: (1) Due to complaints where the loop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Argon Medical Devices Recalled by Argon Medical Devices, Inc Due to There is...
The Issue: There is the potential that the vena Cava Filter may not perform as intended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus BRONCHOFIBERSCOPE BF Type Recalled by Olympus Corporation of the...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA III BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus BRONCHOVIDEOSCOPE Recalled by Olympus Corporation of the Americas...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus Corporation...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus OES BRONCHOFIBERSCOPE BF Type Recalled by Olympus Corporation of the...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus BRONCHOVIDEOSCOPE BF Type Recalled by Olympus Corporation of the...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus EVIS EXERA II BRONCHOVIDEOSCOPE BF TYPE Recalled by Olympus...
The Issue: There have been complaints of endobronchial combustion during therapeutic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Synapsys Informatics Solution Recalled by Becton Dickinson & Co. Due to...
The Issue: There is a risk of mis-association of patient demographic data for users who...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BeamAdjust software Version 2.3.3 The following devices are Recalled by...
The Issue: Generated calibration file will not be correct in case of a relative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FRED Flow Re-Direction Endoluminal Device Recalled by MICROVENTION INC. Due...
The Issue: Intracranial aneurysm flow diverter device may be manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vios Monitoring System Bedside Monitor Recalled by Murata Vios, Inc. Due to...
The Issue: A premature failure condition was identified with the L2050R pulse oximeter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Implant Kit Recalled by...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Catalyft LS Expandable Interbody System Recalled by Medtronic...
The Issue: There is the potential for out of specification device geometries. widths,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.