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. 2,529 recalls have been distributed to District of Columbia in the last 12 months.
Showing 19541–19560 of 47,654 recalls
Recalled Item: Okami brand 8pc Brown Rice Classic California Roll Recalled by Fuji Food...
The Issue: RTE products potentially contaminated with Listeria monocytogenes.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: VCF Vaginal Contraceptive Foam Recalled by Apothecus Pharmaceutical Corp....
The Issue: Defective Delivery System: canister unit exhibiting propellant leakage or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Estriol Recalled by Medisca, Inc. Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride for Injection Recalled by AuroMedics Pharma LLC Due...
The Issue: Discoloration: Product complaints of discoloration after reconstitution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Petroleum jelly (White Petrolatum) USP 100% Recalled by OraLabs,...
The Issue: Cross contamination with other products: undeclared contaminants of phenol...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: bellavista 1000 ventilator Recalled by Vyaire Medical Due to The G6...
The Issue: The G6 bellavista 1000 US ventilators may experience intermittent failures:...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE TUBE Recalled by Greiner Bio-One North America, Inc. Due to The...
The Issue: The Vacuette 3.5mL Serup Sep Clot Activator Tubes may have been damaged at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A2 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carestation 620/650/650c A1 Product Usage: anesthesia systems are intended...
The Issue: GE Healthcare has become aware that there is a potential for a loose cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cios Alpha Recalled by Siemens Medical Solutions USA, Inc Due to During a...
The Issue: During a routine inspection of a system, a crack on the C-arm holder was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Whole Foods Market Raspberry Cheesecake Italian Gelato 1 Pint (473mL)...
The Issue: Undeclared egg
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: LOCATOR OVERDENTURE IMPLANT SYSTEM STERILE R Rx Only QTY 1 . Recalled by...
The Issue: The abutment provided with the Implant System may be out of specification,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXPAREL Recalled by Pacira Pharmaceuticals, Inc. Due to Sub Potent Drug: Out...
The Issue: Sub Potent Drug: Out of Specification (OOS)
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Frog Hollow Holiday Fruitcake Incorrect ingredients: Organic butter Recalled...
The Issue: Customer alerted firm that walnuts were listed on the web page but not in...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ABL90 FLEX Recalled by Radiometer Medical ApS Due to The analyzers fail on...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL90 FLEX PLUS Recalled by Radiometer Medical ApS Due to The analyzers fail...
The Issue: The analyzers fail on S7950 (Range +) QC measurements due to the hemolyzer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 630G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 640G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 620G Insulin Infusion Pump Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic MiniMed 670G System with SmartGuard Recalled by Medtronic Inc. Due...
The Issue: There have been reported incidents of a loose reservoir that can no longer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.