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. 2,552 recalls have been distributed to District of Columbia in the last 12 months.
Showing 17101–17120 of 47,654 recalls
Recalled Item: 9372HD Digital Capture (ver. 1.1.0 + w/ 9263 endoPortal) Recalled by Pentax...
The Issue: There is an intermittent software issue that could affect the systems, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visual-ICE MRI Cryoablation System Mobile Connection Panel (Visual-ICE MRI...
The Issue: Incorrectly installed base.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9310HD Digital Video Capture Module with software version 3.4.0 or Recalled...
The Issue: There is an intermittent software issue that could affect the systems, in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shirakiku brand Black Fungus (Kikurage) Recalled by Wismettac Asian Foods,...
The Issue: California Department of Public Health sampled and tested Shirakiku brand...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Revolution Apex Recalled by GE Healthcare, LLC Due to There is a potential...
The Issue: There is a potential for a smudge artifact that could be suspect for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Artis one systems with a Display Port transceiver-Fluoroscopic X-Ray...
The Issue: Potential malfunction in which the examination room monitor may become...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Trevo XP ProVue Retriever Recalled by Stryker Neurovascular Due to Increase...
The Issue: Increase in fracture complaints of the flexible, tapered core wire,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Genesis (GII) - Product Usage: designed for use in patients Recalled by...
The Issue: The anterior locking detail does not meet its design specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Icono Interventional Fluoroscopic X-Ray system - Product Usage:...
The Issue: There is a software problem which affects the DSA Roadmap application on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NP Thyroid 15 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent Drug:...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NP Thyroid 120 Recalled by Acella Pharmaceuticals, LLC Due to Subpotent...
The Issue: Subpotent Drug: FDA analysis found these products to be less than the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: A Li-Gator Single Use Laparoscopic Clip Applier Recalled by Genicon, Inc....
The Issue: Device malfunction causing the applier to jam, and clip loading failures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofia SARS Antigen FIA Package Insert The Sofia SARS Antigen Recalled by...
The Issue: Instructions for use in the package insert for SARS Antigen FIA test were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nymalize (nimodipine) oral solution Recalled by Arbor Pharmaceuticals Inc....
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Albuterol Sulfate Inhalation Aerosol Recalled by Perrigo Company PLC Due to...
The Issue: Defective Delivery System: Sustained trend of failure to dispense complaints.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MeritMedical Cultura Flex Swab Recalled by Merit Medical Systems, Inc. Due...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Cultura Collection and Transport System Recalled by Merit...
The Issue: The flocked tip of the 100mm swab may break off in the nasophyaryngeal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hurricane RX Biliary Balloon Dilatation Catheter Catalog . M00545890...
The Issue: RX tunnel component (black sheath) may detach from the catheter shaft due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3M Red Dot Monitoring Electrode with Foam Tape - Product Recalled by 3M...
The Issue: Corrosion could cause performance failures in the product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.