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. 2,655 recalls have been distributed to District of Columbia in the last 12 months.
Showing 3141–3160 of 47,654 recalls
Recalled Item: Trader Joe's branded Solid White Albacore Tuna in olive oil Recalled by...
The Issue: Product's easy-pull lid was not secured properly and may cause the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Genova branded Yellowfin Tuna Recalled by Chicken of the Sea; Thai Union Due...
The Issue: Product's easy-pull lid was not secured properly and may cause the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Genova branded Yellowfin Tuna in Extra Virgin Olive Oil and Sea Salt...
The Issue: Product's easy-pull lid was not secured properly and may cause the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Van Camp's branded Solid Light Yellowfin in Vegetable oil Recalled by...
The Issue: Product's easy-pull lid was not secured properly and may cause the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's branded Solid White Albacore Tuna in Water Recalled by Chicken...
The Issue: Product's easy-pull lid was not secured properly and may cause the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's branded Solid White Albacore Tuna in water Recalled by Chicken...
The Issue: Product's easy-pull lid was not secured properly and may cause the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Trader Joe's branded Solid Light Yellowfin Tuna in olive oil Recalled by...
The Issue: Product's easy-pull lid was not secured properly and may cause the product...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Silodosin Capsules Recalled by AvKARE Due to Subpotent Drug: Out of...
The Issue: Subpotent Drug: Out of Specification (OOS) result for De hydro Impurity...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit...
The Issue: Product is mislabeled with the incorrect fill volume.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HemosIL LMW Heparin Controls Recalled by Instrumentation Laboratory Due to...
The Issue: Multiple complaints indicating lower than expected quality control (QC)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioMEMS Heart Failure (HF) System that consist of: -CardioMEMS Hospital...
The Issue: Due to issues associated with data migration of patient information and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fentanyl Transdermal System CII Recalled by Alvogen, Inc Due to Defective...
The Issue: Defective delivery system - patches could be multi-stacked, adhered one on...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Numerous models of nonsterile hemostatic forceps: (1) Recalled by Aesculap...
The Issue: The forceps have been used in ways not covered by the design resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA MR355 Recalled by GE Healthcare (China) Co., Ltd. Due to For certain...
The Issue: For certain MR systems, a scan can be resumed following a Power Monitor trip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed insulin pump Recalled by Medtronic MiniMed, Inc. Due to All...
The Issue: All Medtronic MiniMed pumps (Paradigm series, Minimed 530G, 6XX series, and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.