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. 2,639 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3881–3900 of 47,654 recalls
Recalled Item: BD BACTEC FX Recalled by Becton Dickinson & Co. Due to BD confirmed that...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD MAX System Recalled by Becton Dickinson & Co. Due to BD confirmed that...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cartiva Synthetic Cartilage Implant (SCI) Catalog: CAR-06-US (6mm) Recalled...
The Issue: Patients implanted with synthetic cartilage implant, may experience a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Single User Software Version or Model: 441007 Catalog Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Data Management System Recalled by Becton Dickinson & Co. Due...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA III Gastrointestinal Videoscope GIF-1TH190. Model Number:...
The Issue: High-level disinfection ("HLD") with Acecide-C disinfectant in the Olympus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACTEC 9240 System Version or Model: 445475 Catalog Number: 445475 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR MX Instrument Version or Model: 443989 Catalog Number: 443989...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD EpiCenter Data Management System Version or Model: 440887 Catalog...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD COR PX Instrument Version or Model: 443988 Catalog Number: 443988...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BACTEC FX40 Instrument Version or Model: 442296 Catalog Number: 442296...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BACTEC 9120 System Version or Model: 445570 Catalog Number: 445570 Recalled...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix M50 Automated Microbiology System Version or Model: 443624...
The Issue: BD confirmed that product service credentials used by some BD technical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DesBio lunaSOMM Natural Sleep Support Dietary Supplement capsules Recalled...
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Regadenoson Injection Recalled by Baxter Healthcare Corporation Due to...
The Issue: Labeling: Missing Label
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Offset Cup Impactor - 3/8-16 interface. Reusable surgical instrument used...
The Issue: Recalled lot does not meet specification and has reported incidents of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IBU (ibuprofen) 600 mg tablets Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Tablet/Capsule Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dapsone Gel 7.5% Recalled by VIONA PHARMACEUTICALS INC Due to Crystallization
The Issue: Crystallization
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: CoCr LockingCap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Daytona Small Stature Product Name: Ti Locking Cap 4.5mm...
The Issue: Due to manufacturing defects observed on Locking Caps that affect the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.