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. 2,366 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45701–45720 of 47,654 recalls
Recalled Item: Philips Medical System Extended Brilliance Workspace (EBW) Recalled by...
The Issue: Incorrect values may be displayed. Philips is issuing a software update...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pro Time Microcoagulation System/ Pro Time 3 Cuvette Recalled by...
The Issue: Some Pro Time3 Test Cuvettes within a specified lot range may recover lower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Computed Tomography X-Ray System Recalled by Philips Medical Systems...
The Issue: Philips is issued a Field Change Order to update Extended Brilliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE Parallel Walled Certain Implant Recalled by Biomet...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is Full OSSEOTITE 2 Tapered Certain Implant Recalled by Biomet 3i,...
The Issue: Biomet 3i recalled Full OSSEOTITE 2 Tapered Certain Implant and Full...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes External Fixation System Tube to Tube Clamp Recalled by Synthes USA...
The Issue: The insert provided with the product for the specific lot number indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3 PORT "OFF" MANIFOLD w/WASTE BAG Recalled by ICU Medical, Inc. Due to ICU...
The Issue: ICU Medical, Inc. has identified a potential comingling of components where...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 6.5mm Cancellous Bone Screw Intended to be used for the Recalled by Encore...
The Issue: A product complaint was received where a size 20 screw was labeled as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CYANOCOBALAMIN INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIDAZOLAM HYDROCHLORIDE INJECTION Recalled by Fresenius Kabi USA, LLC Due to...
The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ONDANSETRON INJECTION Recalled by Fresenius Kabi USA, LLC Due to Lack of...
The Issue: Lack of Assurance of Sterility: Glass vials may have finish fractures and...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CellCept (mycophenolate mofetil) capsules Recalled by Genentech, Inc. Due to...
The Issue: Short Fill: some bottles contained less than 120-count per labeled claim.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dr. Reddy's Quetiapine Fumarate Tablets Recalled by Dr. Reddy's...
The Issue: Failed USP Dissolution Test Requirements: During analysis of long term...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Harry & David Creamy Caramel Peanut Spread Recalled by Harry and David...
The Issue: Product received from supplier is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Harry & David Creamy Raspberry Peanut Spread Recalled by Harry and David...
The Issue: Product received from supplier is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Harry & David Creamy Banana Peanut Spread Recalled by Harry and David...
The Issue: Product received from supplier is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Harry & David Crunchy Almond and Peanut Butter Recalled by Harry and David...
The Issue: Product received from supplier is being recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Newman's Own Organics brand Newman-O's Peanut Butter Creme Filled Chocolate...
The Issue: The product was manufactured using peanut butter recalled by Sunland Inc....
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Vacuette Cellestis 1 ml QuantiFERON¿ TB ANTIGEN (HA) High Altitude: Shake...
The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Cellestis 1 ml QuantiFERON¿ - TB ANTIGEN Recalled by Cellestis Inc...
The Issue: Cellestis is recalling QuantiFERON¿¿ - TB Gold TB Blood Collection Tubes and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.