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. 2,429 recalls have been distributed to District of Columbia in the last 12 months.
Showing 36561–36580 of 47,654 recalls
Recalled Item: American Science & Engineering Inc Recalled by American Science &...
The Issue: During factory testing, we discovered that Gemini systems could, in rare...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 0702-001-350Q Recalled by Stryker Instruments Div. of Stryker Corporation...
The Issue: Stryker Instruments is initiating a recall of the Neptune 2 Waste Management...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...
The Issue: There exists a possible position sensor fault in the swivel base axis not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CONTRAVE (naltrexone HCl and bupropion HCl )extended-release tablets...
The Issue: Failed Tablet/Capsule Specifications: Potential tablet defect of broken...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SUCRETS Sore Throat & Cough Vapor Cherry lozenges Recalled by Medtech...
The Issue: Labeling: Label Mix-Up: An incorrect book label for Sucrets Sore Throat,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Exactech Single Barrel Drill Guides The Single Barrel Drill Guide Recalled...
The Issue: Shipped to a single consignee prior to completion of final inspection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Exactech Ambassador Cervical Plate System The Exactech Ambassador Cervical...
The Issue: Shipped to a single consignee prior to completion of final inspection.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Healthcare Diagnostics Dimension Vista Systems Recalled by Siemens...
The Issue: Two software issues may occur in Vista software version 3.6.1. Issue #1:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oncentra Brachy radiation therapy planning software designed to analyze and...
The Issue: Incorrect dose calculation for Regions of Interest (ROIs) defined on a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mycophenolic Acid Delayed-release Tablets Recalled by Mylan Lab Inc Due to...
The Issue: Failed Dissolution Specifications: Low out of specification dissolution results.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NDI Disposable Marker Spheres for Brainlab IGS (Image Guided Recalled by...
The Issue: Inadequate curing of adhesive, which may cause the two halves of the spheres...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NaturaLyte Liquid Bicarbonate Concentrate (Dialysate Concentrate for...
The Issue: Bacterial contamination.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MILEX OMNIFLEX DIAPHRAGM SIZE 80 Model: MXWF80 Recalled by CooperSurgical,...
The Issue: A diaphragm size 80 labeled box was incorrectly packaged with a size 85.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium Sulfate Injection Recalled by Hospira Inc. Due to Failed pH...
The Issue: Failed pH Specifications: 12 month stability testing
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml Recalled by...
The Issue: A reduction in the reconstituted stability has been identified. Clinicians...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Tni-Ultra Assay Recalled by Siemens Healthcare Diagnostics,...
The Issue: System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Instrument Series 240 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CentraLink" Data Management System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has determined that the sample query function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Instrument Series 528 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROXYZINE HYDROCHLORIDE (STERILE WATER) (10ML VIAL) 25MG/ML INJECTABLE...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.