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. 2,591 recalls have been distributed to District of Columbia in the last 12 months.
Showing 11021–11040 of 27,451 recalls
Recalled Item: Tosoh Bioscience AIA- PACK HCG Calibrator Set-In Vitro Diagnostic for...
The Issue: Decreased stability for five (5) lots of Calibrator Sets and Calibration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accelerator a3600 system with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aptio Automation systems with Sysmex XN-9000/XN-9100 Interface Module (dual...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WallFlexTM Biliary RX Fully Covered Stent System RMV (10mmx60mm Stent)...
The Issue: Mislabeled: WallFlex Biliary RX Uncovered Stent System 10x60mm devices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FlexLab (FLX) with Sysmex XN-9000/XN-9100 Interface Module (dual robot)...
The Issue: Firmware of the Sysmex XN-9000/XN-9100 Interface Module (IM) and of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PC Application Software c4D as part of the device Catalyst: Recalled by...
The Issue: PC Application Software c4D not changing Site upon synchronization during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss Meditec AG VISUREF150 - Product Usage: Recalled by Carl Zeiss...
The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carl Zeiss Meditec Ag VISULENS 550 - Product Recalled by Carl Zeiss Meditec...
The Issue: Due to the incorrect DC/DC converter being assembled onto the communication...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Talladium Luminesse Zirconia Discs Recalled by Talladium Inc Due to The...
The Issue: The linear shrinkage on the zirconia blank disc s part label is incorrect....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Positron Emission Tomography and Computed Tomography System Recalled by...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Shanghai United Imaging...
The Issue: A potential issue of an incorrect CT scan delay timer to be displayed on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Panther Fusion Tube Tray Recalled by Hologic, Inc Due to Tube trays may leak...
The Issue: Tube trays may leak which could invalidate patient results or assay...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Padgett Dermatome Set - Product Usage: are intended for Recalled by...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13 ft Handpiece Cable Recalled by Integra LifeSciences Corp. Due to lntegra...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Padgett Electric Dermatome Set - Product Usage: are intended...
The Issue: lntegra LifeSciences has identified through a number of complaints that the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System PC Unit Model 8100 (Pump Module) and Recalled by CareFusion...
The Issue: Pump Module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris System PC Unit Model 8015 Recalled by CareFusion 303, Inc. Due to The...
The Issue: The pump module keypad may exhibit keys that are unresponsive or stuck as a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris System Recalled by CareFusion 303, Inc. Due to The Alaris PC unit...
The Issue: The Alaris PC unit can display incorrect syringe type and/or syringe sizes....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.