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. 1,649 recalls have been distributed to District of Columbia in the last 12 months.
Showing 43241–43260 of 47,654 recalls
Recalled Item: NeoCitran DM Cough & Cold (dextromethorphan hydrobromide 30 mg Recalled by...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Multi-Symptom Severe Cold (acetaminophen 500 mg Recalled by...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Daytime Severe Cold & Cough (acetaminophen 650 mg Recalled by...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Cold and Flu (acetaminophen 325 mg Recalled by Novartis Consumer...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Sugar-Free Nighttime Severe Cold & Cough (acetaminophen 650 mg...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Theraflu Severe Cold & Cough powder packets containing Daytime formula...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NeoCitran Extra Strength Cold & Flu (acetaminophen 650 mg Recalled by...
The Issue: Presence of Foreign Substance: The products are being recalled because they...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: LifeShield Recalled by Hospira Inc. Due to Hospira has received reports of...
The Issue: Hospira has received reports of customers experiencing air-in-line alarms...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris PC unit Recalled by CareFusion 303, Inc. Due to CareFusion is...
The Issue: CareFusion is recalling the Alaris PC units model 8015 (PC unit), version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GN Kit (Catalog number 20-005-021) Recalled by Nanosphere, Inc....
The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Verigene BC-GP Kit (Catalog number 20-005-018) Recalled by Nanosphere, Inc....
The Issue: There is a specific Extraction Tray lot containing Tips that may slightly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ENTERIC COATED ASPIRIN (NSAID) Recalled by Advance Pharmaceutical Inc Due to...
The Issue: Labeling: Label Mix-Up: A complaint from a pharmacist was received that the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The SurgiCounter Charging Cradle Product Usage: SurgiCounter Charging...
The Issue: Faulty SurgiCounter Charging Cradle can prevent the scanner from charging or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Streamline MIS Spinal Fixation System Fixed Rod Holder NON STERILE Recalled...
The Issue: The affected fixed rod holders did not allow the instrument to lock down on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: bioMerieux Vitek 2 Systems Software version 6.01 software Recalled by...
The Issue: A product issue has been identified for customers using software version...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.