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 45261–45280 of 47,654 recalls
Recalled Item: PredniSONE Tablets Recalled by West-ward Pharmaceutical Corp. Due to...
The Issue: Presence of Foreign Substance: A complaint was received for black specks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Outlook ES pump is intended for use with B. Braun Recalled by B Braun...
The Issue: B. Braun Medical Inc. is informing our customers of a field correction...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Canon Full Auto RK-F2 Recalled by Canon Inc. Due to Canon Inc. had received...
The Issue: Canon Inc. had received 17 claims from our foreign sales companies between...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Companion External Battery Recalled by SynCardia Systems Inc. Due to...
The Issue: Syncardia Systems is recalling the Companion External Batteries used with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cyanocobalamin 1000 mcg/ml Recalled by Green Valley Drugs Due to...
The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methylprednisolone Preservative Free 40 mg/ml Injectible Suspension Recalled...
The Issue: Non-Sterility: Green Valley Drugs received positive sterility results from...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...
The Issue: Failed Dissolution Specifications: The affected lots may not meet the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...
The Issue: Failed Dissolution Specifications: The affected lots may not meet the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dextroamphetamine Sulfate Extended Release Capsules Recalled by Amedra...
The Issue: Failed Dissolution Specifications: The affected lots may not meet the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Synthroid (Levothyroxine Sodium) tablets Recalled by Abbott Laboratories Due...
The Issue: Labeling: Error on Declared Strength. Product labeled to contain 150 mcg...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Clean & Clear advantage Recalled by Johnson & Johnson Due to Superpotent...
The Issue: Superpotent (Single Ingredient Drug): salicylic acid
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Abbott m2000sp Instrument Recalled by Abbott Molecular Due to An issue with...
The Issue: An issue with the m2000sp Instrument software has been identified whereby,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quidel Recalled by Quidel Corporation Due to Quidel Corporation has...
The Issue: Quidel Corporation has initiated a voluntary recall of specific lots of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS 8IN CALC 1.5/18.0 Packaging: Product is packed within Recalled by...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS L 9IN CALC 2.25/15.0 Packaging: Product is packed Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS R 9IN CALC 2.25/16.5 Packaging: Product is packed Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS 8IN CALC 1.5/19.5 Packaging: Product is packed within Recalled by...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS L 9IN CALC 2.25/19.5 Packaging: Product is packed Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic has...
The Issue: Medtronic has identified 140 Restore DBS Extension Kits (model numbers 7482,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOL SYS F 8 CALC 13.5MM LG Packaging: Product is Recalled by DePuy...
The Issue: An Engineering Analysis has determined the Solution Calcar Stem has the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.