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. 891 recalls have been distributed to District of Columbia in the last 12 months.
Showing 45541–45560 of 47,654 recalls
Recalled Item: Gluten Free Cafe Cinnamon Sesame Bar. The Retail Carton has Recalled by...
The Issue: Gluten Free Cafe Cinnamon Sesame Bar is recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Gluten Free Cafe Chocolate Sesame Bar. The Retail Carton has Recalled by...
The Issue: Gluten Free Cafe Chocolate Sesame Bar is recalled due to the potential to be...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dannon Activia LIGHT Nonfat Yogurt Strawberry / Blueberry Flavor 12-4oz...
The Issue: The recalled products may potentially contain metal fragment(s) from a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Frozen Tuna Loins 3/5 Recalled by Unified Seafood Company., Inc. Due to...
The Issue: Unified Seafood Co is recalling Frozen Yellowfin Tuna Loin 3/5 due to...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Swanson Organic Recalled by Swanson Health Products, Inc Due to This is to...
The Issue: This is to inform you of a product recall involving 2 lots of Swanson...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Dannon Activia LIGHT Nonfat Yogurt Peach Flavor 4x4oz cups INGREDIENTS:...
The Issue: The recalled products may potentially contain metal fragment(s) from a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ESTEE LAUDER DayWear Sheer Tint Release Recalled by Estee Lauder Inc Due to...
The Issue: Failed Stability Specifications: The active sunscreen ingredient, avobenzone...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dannon Light & Fit Carb & Sugar Control Cultured Dairy Recalled by The...
The Issue: The recalled products may potentially contain metal fragment(s) from a...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Accolade TMZF Plus 127 degree Neck Angle V40 Hip Stem Recalled by Stryker...
The Issue: Stryker has received a report that single size 3.5 stem was packaged as size...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Siemens Symbia S series is intended to aid in detecting Recalled by...
The Issue: There is a potential for the linear bearing car to fail allowing the ball...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Siemens Symbia T series is intended to aid in detecting Recalled by...
The Issue: There is a potential for the linear bearing car to fail allowing the ball...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HEXTEND 6% Hetastarch in Lactated Electrolyte Injection Recalled by Hospira...
The Issue: Lack of Assurance of Sterility: There is the potential for the solution to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Classic Zi Xiu Tang Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ultimate Formula Recalled by Zi Xiu Tang Success, LLC Due to Undeclared...
The Issue: Marketed Without An Approved NDA/ANDA: Products were found to contain...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Alere Cholestech LDX Multianalyte Control Recalled by Alere San Diego, Inc....
The Issue: Out of range (increased) HDL Cholesterol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Calibration Verification Recalled by Alere San Diego,...
The Issue: Out of range (increased) HDL Cholesterol results.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD BBL Taxo XV Factor Strips Recalled by Becton Dickinson & Co. Due to In...
The Issue: In vitro diagnostic test kit was not manufactured according to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS AdVance" Male Sling System 720088-01 AMS AdVance" Male Sling Recalled by...
The Issue: American Medical Systems¿ (AMS) is issuing a voluntary recall on a number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMRIS ORT100 (Part Number 110470-000) and ORT200 (Part Number 112216-00)...
The Issue: IMRIS Inc. initiated a recall of their OR Tables ORT100 and ORT200. When...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Titan Spine Endoskeleton TA Implant products. 2107-0118 18mm Standard...
The Issue: Titan Spine LLC, is conducting a recall on the Endoskeleton TA VBR products....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.