Product Recalls in District of Columbia
Product recalls affecting District of Columbia — including food, drugs, consumer products, medical devices, and vehicles distributed to District of Columbia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,629 recalls have been distributed to District of Columbia in the last 12 months.
Showing 5881–5900 of 27,451 recalls
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: VITROS Immunodiagnostic Products Troponin I ES Reagent Pack Recalled by...
The Issue: Reagent packs could potentially contain incorrect wells, which will generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Troponin I ES Calibrators Recalled by...
The Issue: Reagent packs could potentially contain incorrect wells, which will generate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Hybrid Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Select VA 21 with FD- A Mobile X-ray system Recalled by Siemens Medical...
The Issue: Incorrect glue was applied on the plexiglass sheet on the single tank cover...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cardiosave Rescue Intra-Aortic Balloon Pump (IABP) Recalled by Datascope...
The Issue: IABP may lose the ability to charge batteries in one or both bay slots....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.