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. 2,448 recalls have been distributed to District of Columbia in the last 12 months.
Showing 30101–30120 of 47,654 recalls
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Temozolomide Capsules Recalled by Mylan LLC. Due to Failed Tablet/Capsule...
The Issue: Failed Tablet/Capsule Specifications: customer complaints of broken or...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smoked Chipotle Flavored Kettle Cooked Potato Chips 2.625 oz and 8.0 oz...
The Issue: Herrs Foods is announcing a product recall on Chipotle flavored Kettle...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dried Smoke Chipotle Flavored Kettle Cooked Potato Chips 2.0 oz. Recalled by...
The Issue: Herrs Foods is announcing a product recall on Chipotle flavored Kettle...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Eclipse Hypodermic Needle Recalled by Becton Dickinson & Company Due to BD...
The Issue: BD is initiating a Product Advisory for the Eclipse Hypodermic Needle...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Comprehensive Reverse Shoulder System Humeral Tray Model 115340 Recalled by...
The Issue: Higher than anticipated rate of fracturing due to design. Risk of revision...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Na+ Slides Recalled by Ortho-Clinical Diagnostics Due to There is a...
The Issue: There is a potential for biased results to be generated over the 10 day...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accu-Chek Connect Diabetes Management App Recalled by Roche Diabetes Care,...
The Issue: iOS and Android: Under certain conditions the affected app versions may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aripiprazole Tablets Recalled by Apotex Inc. Due to Superpotent Drug:...
The Issue: Superpotent Drug: Product may not meet specifications throughout shelf life.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: RingLoc ArComXL Highly Crosslinked Polyethylene Liners ArComXL High Wall...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Active Articulation ArComXL Polyethylene Bearings Active Articulation...
The Issue: Product complaints indicated that the part and lot numbers on the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DxH 600 Coulter Cellular Analysis System Recalled by Beckman Coulter Inc....
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SafeStep¿ Huber Needle Set with Y-Injection Site. Product Code: LH-0029YN....
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC 9800. MDL Numbers: D222250 Recalled by GE OEC Medical Systems, Inc Due...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniLoc¿ Safety Infusion Set Winged without Y-Injection Site. Product Code:...
The Issue: Bard Access Systems announces a voluntary field action for the SafeStep¿...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OEC MiniView 6800. MDL Number: D002533 The OEC MiniView 6800 Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: UniCel DxH 800 Coulter Cellular Analysis System Recalled by Beckman Coulter...
The Issue: Beckman Coulter has determined that additional clarification for the Blast...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The OEC 9900 Elite mobile fluoroscopy system is designed to Recalled by GE...
The Issue: GE Healthcare Surgery announces a voluntary field action for the OEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium for Injection Recalled by Aurobindo Pharma USA Inc Due...
The Issue: Discoloration: Some vials were found to contain powder with a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MIDAZOLAM INJECTION Recalled by Fresenius Kabi USA, LLC Due to Failed...
The Issue: Failed Impurities/Degradation Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.