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. 2,542 recalls have been distributed to District of Columbia in the last 12 months.
Showing 16001–16020 of 27,451 recalls
Recalled Item: ACUSON SC2000 Ultrasound System Product Usage: The SC2000 ultrasound imaging...
The Issue: The application may underestimate the EROA (Effective Regurgitant Orifice...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biograph Horizon - PET/CT Recalled by Siemens Medical Solutions USA, Inc....
The Issue: Error introduced into PET images acquired and reconstructed with VJ20A...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux VITEK 2 Gram Positive Cefoxitin Screen Recalled by bioMerieux,...
The Issue: Customer reports indicated an increase in the rate of non-detected MRSA in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity Universal Viewer Product Usage: Usage: Centricity PACS-IW with...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Centricity PACS-IW with Universal Viewer Product Usage: Usage: Centricity...
The Issue: Potential that one or more image series may be missing from an exam without...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: O-arm 1000 mobile image-intensified fluoroscopic x-ray system Recalled by...
The Issue: Software update ("SW Update 3.2.1") is being implemented to address the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Liberty Select Cycler (SW v.2.8.7) Recalled by Fresenius Medical Care Renal...
The Issue: The recalling firm identified a software issue related to the Patient Line...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioM¿rieux VITEK 2 NH ID Test Kit Product Usage: Is Recalled by Biomerieux...
The Issue: Missing desiccant.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Bair Hugger(M) Normothermia System Recalled by 3M Company - Health Care...
The Issue: Adesign change to 3M(TM) Bair Hugger(TM) Full Access Underbody Warming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo XT Suture Anchor Recalled by Valeris Medical, LLC Due to The label on...
The Issue: The label on Apollo XT 5.5mm Suture Anchor (part # XTS-5515; lots 2358,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The FEMTO LDV(TM)Z8 Femtosecond Surgical Laser The FEMTO LDV(TM)Z8...
The Issue: This Correction is being initiated based on a customer complaint received on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AutoMate 2550 "High Speed" Catalog Number ODL25255 Recalled by Beckman...
The Issue: A misaligned pipette tip sensor poses the remote risk of cross-contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope URF-P6 Recalled by Olympus Corporation of the...
The Issue: Breakage of the endoscope's insertion tube bending section during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno videoscope URF-V2 Uretero-reno videoscope URF-V2R Recalled by...
The Issue: Potential breakage of the endoscope s insertion tube bending section during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uretero-reno fiberscope URF-P6RP6 Recalled by Olympus Corporation of the...
The Issue: Breakage of the endoscope's insertion tube bending section during surgical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Progressa Bed - AC-powered adjustable hospital bed Recalled by Hill-Rom,...
The Issue: A component used within the braking system may break resulting in one or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sonialvision Safire II Recalled by Shimadzu Medical Systems Due to When...
The Issue: When selecting serial radiography with a pulse rate of 7.5fps (including...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COULTER EPICS XL Flow Cytometer COULTER EPICS XL-MCL Flow Cytometer Recalled...
The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Cytomics FC 500 With CXP Software BECKMAN COULTER 2) Recalled by Beckman...
The Issue: A manufacturing defect on the amplifier board of the Flow Cytometers my...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.