Product Recalls in Washington
Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,798 recalls have been distributed to Washington in the last 12 months.
Showing 9021–9040 of 51,768 recalls
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: 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.
Recalled Item: OmniTom/OmniTom Elite- X-ray computed tomography applications for anatomy...
The Issue: 1. Wheels loosening over time with use of the device could lead to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StellaLife VEGA Oral Care Rinse Recalled by Homeocare Laboratories, Inc. Due...
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Arnica 7 Cream Recalled by Homeocare Laboratories, Inc. Due to cGMP deviations
The Issue: cGMP deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.