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 29261–29280 of 47,654 recalls
Recalled Item: ESTRIOL Recalled by Medisca, Inc. Due to cGMP Deviations; manufacturer...
The Issue: cGMP Deviations; manufacturer initiated recall of API product after...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Mederi Stretta Catheter and Accessory Kit Recalled by Mederi Therapeutics,...
The Issue: Product sterility compromised due to breach in sterile barrier package
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Second generation neoBLUE LED Phototherapy Light (neoBLUE 2) sold between...
The Issue: The second generation neoBLUE 2 lights with a black band, sold from 2003 to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AQUIOS CL Flow Cytometer Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter has confirmed that the Export feature located in the Results...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Value Bread and Butter Chips 24 Fl Oz. Distributed by: Wal-Mart Stores...
The Issue: Glass fragments were found in Great Value Bread and Butter Chips.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Premium Hunt's Chili Kit Recalled by ConAgra Foods Inc Due to Potential...
The Issue: Potential Salmonella contamination of spice packet within chili kits.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Arctic Sun 5000 Temperature Management System Recalled by C.R. Bard, Inc....
The Issue: Potential failure of the Arctic Sun 5000 Temperature Management System may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Disposable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ATAR Reusable Extension Cable Recalled by Oscor, Inc. Due to The Reusable...
The Issue: The Reusable Oscor ATAR extension cables could separate from the connector...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alka-Seltzer Original ( 325 mg Aspirin (NSAID) Recalled by Bayer HealthCare...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alka-Seltzer Gold (1000 mg Anhydrous citric acid Recalled by Bayer...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alka-Seltzer Extra Strength (500 mg Aspirin (NSAID) Recalled by Bayer...
The Issue: Defective Container: Confirmed customer compliant of small holes or cracks...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Optional MDRC-1119 Front Cover Attachment Kit for review display monitors....
The Issue: If metal strips are removed and re-applied to another display, there is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RENOVATION Recalled by Smith & Nephew, Inc. Due to The stability data does...
The Issue: The stability data does not support the product labeled with a 10-year shelf...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Knee/Shldr Recalled by Breg Inc Due to They may not have been...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Shldr XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing M/U XL Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Recalled by Breg Inc Due to They may not have been sealed prior to...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressing Back Recalled by Breg Inc Due to They may not have been sealed...
The Issue: They may not have been sealed prior to sterilization. Products with unsealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.