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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 26241–26260 of 27,451 recalls
Recalled Item: ADVIA Centaur Ferritin Calibrator C-Used with the ADVIA Centaur Ferritin...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Calibrator C-Used with the ADVIA Centaur Ferritin assay...
The Issue: Ferritin Analytical Sensitivity and Calibrator C Realignment with kit lots...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Membrane units for E7077 Electrode Radiometer Medical ApS. The...
The Issue: RADIOMETER became aware that some membranes may have enzyme residue on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista(R) IRON Flex(R) reagent cartridge (K3085) The IRON method...
The Issue: Siemens Healthcare Diagnostics has confirmed the potential for falsely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo WorkFlow SLR Recalled by Siemens Medical Solutions USA, Inc...
The Issue: Under certain conditions, when using the Search functionality, the potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The touchscreen display (model 94267) designed for use with the Recalled by...
The Issue: Potential failure of Spacelabs Healthcare Touchscreen Display, Model 94267...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caddy - PedFuse Recalled by SpineFrontier, Inc. Due to Two sections that are...
The Issue: Two sections that are designated for the 8mm and 9mm screws were switched;...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle3 VCC P/N 4598 001 41341 REV A Recalled by Philips Medical Systems...
The Issue: Philips Medical Systems Cleveland), Inc. is recalling Pinnacle3 Virtual...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ranawat/Burnstein Acetabular Shell 54mm/Limited Holes/Porous Coated is a...
The Issue: The color code on label conflicts with the liner size (liner size 24 should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: West Nile Virus IgG DxSelect" kit Catalog No. EL0300G Kit Lots 122150...
The Issue: The firm recalled due to higher reactivity with some samples in the effected...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD CYCLESURE 24 Biological Indicator (BI) product Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) is recalling all lots of Sterrad...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Repeater Pump Recalled by Baxa Corporation Due to The firm is issuing a...
The Issue: The firm is issuing a field correction to the operators manual included with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Case Carton: BD Oral Dispensing Syringe 1 mL Clear with Tip Cap BD Recalled...
The Issue: BD received a complaint report for mixed syringe tips (oral and non-oral...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Cardio Imaging 5.0 is a software only Picture Archiving Recalled...
The Issue: GE Healthcare is aware of a potential safety risk where an image labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Polaris 5.5 Button Lock Screw Inserter. Catalog number 14-500178...
The Issue: Broken screw insertor hardness was measured and found to be below the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) BenchMark ULTRA Recalled by Ventana...
The Issue: Potiential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...
The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VENTANA (a member of the Roche Group) DISCOVERY ULTRA Recalled by Ventana...
The Issue: Potential for a waste fluid overflow condition to accur while running...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.