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. 2,423 recalls have been distributed to District of Columbia in the last 12 months.
Showing 37261–37280 of 47,654 recalls
Recalled Item: Cranberry Health Mix: America Choice Recalled by Aurora Products, Inc. Due...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Forest Bounty Grail Mix: Aurora Recalled by Aurora Products, Inc. Due to...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Salt Mixed Nuts: Aurora Recalled by Aurora Products, Inc. Due to...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 5 K Omega Trail Mix: Aurora 20 oz. Plastic Cup Recalled by Aurora Products,...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: San Fernando Sunshine Mix: Gourmet Garage Recalled by Aurora Products, Inc....
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Deluxe Mixed Nuts No Salt: Aurora Recalled by Aurora Products, Inc. Due to...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Raisin Nut Party Mix: Aurora Recalled by Aurora Products, Inc. Due to...
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Deluxe Mixed Nuts with Sea Salt: Aurora Recalled by Aurora Products, Inc....
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Roasted Mixed Nuts No Salt: Gourmet Garage Recalled by Aurora Products, Inc....
The Issue: Salmonella
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Axis-Shield Liquid Stable (LS) 2-Part HOMOCYSTEINE REAGENT Recalled by...
The Issue: Deterioration in performance of the Liquid Stable (LS) 2-Part HOMOCYSTEINE...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carter-Thomason II Port Closure System Recalled by CooperSurgical, Inc. Due...
The Issue: The pad printing around the suture entry holes on the 15mm Suture Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMARTABLATE RF Generator System Recalled by Biosense Webster, Inc. Due to...
The Issue: Biosense Webster is recalling the SMARTABLATE Generator System because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARBOplatin Injection 450 mg/45 mL (10 mg/mL) Recalled by Mylan...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Methotrexate Injection Recalled by Mylan Institutional LLC Due to Presence...
The Issue: Presence of Particulate Matter
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 5% Dextrose Injection Recalled by Baxter Healthcare Corp. Due to Lack of...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...
The Issue: Lack of Assurance of Sterility. Complaints were receive of missing closures...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...
The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: SULFAMETHOXAZOLE AND TRIMETHOPRIM ORAL SUSPENSION Recalled by Akorn, Inc....
The Issue: Failed Dissolution Specifications: Out of specification for dissolution of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.